A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694699



Internal ID15431351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95290849..95299648hg38UCSC Ensembl
Innerchr15:95834078..95842877hg19UCSC Ensembl
Innerchr15:93635082..93643881hg18UCSC Ensembl
Innerchr15:93635082..93643881hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg388800
hg198800
hg188800
hg178800
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521930
Supporting Variants
Samples
Known GenesLOC400456
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694699
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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