A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704460



Internal ID15441112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61390735..61406976hg38UCSC Ensembl
Innerchr15:61682934..61699175hg19UCSC Ensembl
Innerchr15:59470226..59486467hg18UCSC Ensembl
Innerchr15:59470226..59486467hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3816242
hg1916242
hg1816242
hg1716242
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527951
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704460
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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