A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700837



Internal ID15437489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85919621..85940447hg38UCSC Ensembl
Innerchr15:86462852..86483678hg19UCSC Ensembl
Innerchr15:84263856..84284682hg18UCSC Ensembl
Innerchr15:84263856..84284682hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3820827
hg1920827
hg1820827
hg1720827
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524836
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700837
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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