A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579431



Internal ID16020154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36352224..36356091hg38UCSC Ensembl
Innerchr19:36843126..36846993hg19UCSC Ensembl
Innerchr19:41534966..41538833hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383868
hg193868
hg183868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899078, nssv899001, nssv899031, nssv899034, nssv899087, nssv899053, nssv899043, nssv899015, nssv899074, nssv898992, nssv899042, nssv899014, nssv899037, nssv899036, nssv899067, nssv899035, nssv899056, nssv899077, nssv899019, nssv898993, nssv899010, nssv899061, nssv899082, nssv899075, nssv899041, nssv899025, nssv899002, nssv899083, nssv899011, nssv899026, nssv899005, nssv899023, nssv899059, nssv899070, nssv899007, nssv899008, nssv899081, nssv899080, nssv899040, nssv898994, nssv899055, nssv899009, nssv898995, nssv899079, nssv899029, nssv899052, nssv899086, nssv899030, nssv899072, nssv899065, nssv899044, nssv899058, nssv899024, nssv899022, nssv899071, nssv899018, nssv899076, nssv899062, nssv899012, nssv899004, nssv898997, nssv899016, nssv899013, nssv899049, nssv899073, nssv899000, nssv898998, nssv899066, nssv899046, nssv899064, nssv899039, nssv899068, nssv899003, nssv899085, nssv899032, nssv899017, nssv899050, nssv899060, nssv899091, nssv899088, nssv899057, nssv899090, nssv899089, nssv899063, nssv898996, nssv899092, nssv899033, nssv899048, nssv899020, nssv899084, nssv899006, nssv898999, nssv899045, nssv899051, nssv899069, nssv899054, nssv899021, nssv899047, nssv899027, nssv899038, nssv899028
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579431
Frequency
Sample Size17421
Observed Gain0
Observed Loss101
Observed Complex0
Frequencyn/a


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