A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149261



Internal ID15880730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87256693..87320484hg38UCSC Ensembl
Innerchr15:87799924..87863715hg19UCSC Ensembl
Innerchr15:85600928..85664719hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3863792
hg1963792
hg1863792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570364
Supporting Variants
SamplesNINDS_258
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149261
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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