A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579461



Internal ID16020184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36834924..37256206hg38UCSC Ensembl
Innerchr19:37325826..37747108hg19UCSC Ensembl
Innerchr19:42017666..42438948hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38421283
hg19421283
hg18421283
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899148
Samples
Known GenesZNF345, ZNF383, ZNF420, ZNF568, ZNF585A, ZNF585B, ZNF790, ZNF829
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579461
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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