A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148658



Internal ID15879228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23403645..23474682hg38UCSC Ensembl
Innerchr15:23648792..23719829hg19UCSC Ensembl
Innerchr15:21200233..21270922hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3871038
hg1971038
hg1870690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568310
Supporting Variants
SamplesHGDP01330
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148658
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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