A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578796



Internal ID16366205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19727512..19728217hg38UCSC Ensembl
Innerchr19:19838321..19839026hg19UCSC Ensembl
Innerchr19:19699321..19700026hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38706
hg19706
hg18706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896121, nssv896002, nssv896147, nssv896016, nssv896093, nssv896104, nssv895994, nssv896119, nssv895976, nssv896087, nssv896145, nssv896122, nssv896053, nssv896018, nssv896071, nssv896005, nssv896134, nssv896124, nssv896076, nssv895963, nssv896146, nssv895996, nssv895981, nssv896052, nssv895978, nssv896138, nssv896068, nssv896118, nssv895983, nssv896129, nssv896020, nssv895998, nssv896080, nssv896047, nssv896036, nssv896033, nssv896144, nssv896058, nssv896050, nssv895966, nssv896115, nssv896116, nssv896042, nssv896099, nssv896014, nssv896017, nssv895975, nssv896022, nssv896004, nssv896012, nssv896007, nssv896106, nssv896137, nssv895997, nssv895985, nssv896084, nssv896073, nssv896086, nssv896015, nssv895969, nssv896081, nssv896141, nssv896114, nssv896056, nssv896103, nssv896090, nssv895986, nssv895970, nssv896066, nssv896126, nssv896094, nssv896000, nssv895992, nssv896109, nssv896065, nssv896132, nssv896101, nssv895961, nssv896078, nssv896069, nssv896117, nssv896019, nssv896049, nssv896044, nssv896039, nssv896107, nssv895958, nssv896095, nssv896038, nssv896030, nssv895991, nssv896035, nssv896041, nssv896034, nssv896051, nssv896092, nssv896028, nssv896045, nssv895988, nssv896139, nssv895999, nssv896027, nssv896142, nssv896040, nssv896032, nssv896089, nssv895959, nssv896088, nssv895989, nssv896131, nssv896130, nssv896064, nssv896102, nssv895995, nssv895972, nssv895965, nssv895973, nssv896070, nssv895968, nssv896082, nssv896063, nssv896110, nssv895977, nssv895971, nssv896061, nssv896136, nssv896011, nssv896105, nssv895974, nssv895964, nssv896001, nssv896113, nssv896085, nssv896062, nssv896010, nssv896133, nssv896054, nssv896072, nssv896083, nssv895960, nssv895962, nssv896077, nssv896123, nssv896091, nssv896067, nssv896023, nssv896108, nssv896100, nssv896143, nssv896025, nssv896013, nssv896048, nssv896140, nssv896060, nssv896079, nssv896055, nssv896096, nssv896128, nssv896112, nssv896006, nssv896046, nssv896057, nssv896135, nssv896097, nssv896125, nssv896043, nssv895990, nssv896009, nssv895979, nssv896008, nssv896021, nssv895993, nssv895987, nssv895980, nssv896075, nssv895984, nssv896074, nssv896003, nssv896037, nssv896029, nssv896111, nssv895967, nssv896026, nssv896120, nssv896059, nssv896031, nssv896127, nssv896098, nssv895982, nssv896024
Samples
Known GenesZNF14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578796
Frequency
Sample Size17421
Observed Gain0
Observed Loss190
Observed Complex0
Frequencyn/a


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