A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578926



Internal ID16019649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20643886..20858544hg38UCSC Ensembl
Innerchr19:20826692..21041350hg19UCSC Ensembl
Innerchr19:20618532..20833190hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38214659
hg19214659
hg18214659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6318n54
Supporting Variantsnssv1150128
Samples1780862577_A
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578926
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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