A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699117



Internal ID15435769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69819234..69849566hg38UCSC Ensembl
Innerchr15:70111573..70141905hg19UCSC Ensembl
Innerchr15:67898627..67928959hg18UCSC Ensembl
Innerchr15:67898627..67928959hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3830333
hg1930333
hg1830333
hg1730333
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523368
Supporting Variants
Samples
Known GenesLINC00593
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699117
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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