A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149553



Internal ID15531836
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 StatusS
Merged Variantsnsv568761
Supporting Variants
SamplesHGDP01214
Known GenesHERC2P10, LOC100288637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149553
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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