A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568761



Internal ID16009484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30644082..30831032hg38UCSC Ensembl
Innerchr15:30936285..31123235hg19UCSC Ensembl
Innerchr15:28723577..28910527hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38186951
hg19186951
hg18186951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4425n54
Supporting Variantsnssv1149553
SamplesHGDP01214
Known GenesHERC2P10, LOC100288637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568761
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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