A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568760



Internal ID16009483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30644082..30825200hg38UCSC Ensembl
Innerchr15:30936285..31117403hg19UCSC Ensembl
Innerchr15:28723577..28904695hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38181119
hg19181119
hg18181119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4425n54
Supporting Variantsnssv839488
Samples
Known GenesHERC2P10, LOC100288637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568760
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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