A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696765



Internal ID15433417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:47173502..47180971hg38UCSC Ensembl
Innerchr15:47465699..47473168hg19UCSC Ensembl
Innerchr15:45252991..45260460hg18UCSC Ensembl
Innerchr15:45252991..45260460hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg387470
hg197470
hg187470
hg177470
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519284
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696765
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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