A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698546



Internal ID15088512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56070770..56076926hg38UCSC Ensembl
Innerchr15:56362968..56369124hg19UCSC Ensembl
Innerchr15:54150260..54156416hg18UCSC Ensembl
Innerchr15:54150260..54156416hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386157
hg196157
hg186157
hg176157
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522888
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698546
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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