A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574110



Internal ID16361519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:948888..952193hg38UCSC Ensembl
Innerchr17:852128..855433hg19UCSC Ensembl
Innerchr17:798878..802183hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg383306
hg193306
hg183306
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5396n54
Supporting Variantsnssv866064, nssv866031, nssv866070, nssv866036, nssv866085, nssv866032, nssv866046, nssv866076, nssv866041, nssv866068, nssv866047, nssv866060, nssv866050, nssv866030, nssv866075, nssv866087, nssv866082, nssv866057, nssv866033, nssv866071, nssv866067, nssv866069, nssv866079, nssv866077, nssv866039, nssv866061, nssv866045, nssv866073, nssv866038, nssv866052, nssv866049, nssv866083, nssv866053, nssv866056, nssv866055, nssv866035, nssv866078, nssv866080, nssv866042, nssv866081, nssv866063, nssv866040, nssv866062, nssv866054, nssv866044, nssv866065, nssv866059, nssv866084, nssv866048, nssv866034, nssv866037, nssv866072, nssv866066, nssv866051, nssv866086, nssv866088, nssv866074, nssv866058, nssv866043
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574110
Frequency
Sample Size17421
Observed Gain56
Observed Loss3
Observed Complex0
Frequencyn/a


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