A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702588



Internal ID15439240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17604390..17610204hg38UCSC Ensembl
Innerchr11:17625937..17631751hg19UCSC Ensembl
Innerchr11:17582513..17588327hg18UCSC Ensembl
Innerchr11:17582513..17588327hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg385815
hg195815
hg185815
hg175815
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520453
Supporting Variants
Samples
Known GenesOTOG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702588
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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