A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578918



Internal ID16019641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20606450..20825406hg38UCSC Ensembl
Innerchr19:20789256..21008212hg19UCSC Ensembl
Innerchr19:20581096..20800052hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38218957
hg19218957
hg18218957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6318n54
Supporting Variantsnssv896521
Samples
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578918
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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