A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578931



Internal ID16019654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20651291..20804744hg38UCSC Ensembl
Innerchr19:20834097..20987550hg19UCSC Ensembl
Innerchr19:20625937..20779390hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38153454
hg19153454
hg18153454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6319n54
Supporting Variantsnssv896552, nssv896553, nssv1150131, nssv896551, nssv896554, nssv1150130, nssv896550, nssv896555, nssv1150129
SamplesNINDS_110, 1780862408_A, 1780854063_A
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578931
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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