A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700876



Internal ID15437528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92147318..92160950hg38UCSC Ensembl
Innerchr15:92690548..92704180hg19UCSC Ensembl
Innerchr15:90491552..90505184hg18UCSC Ensembl
Innerchr15:90491552..90505184hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3813633
hg1913633
hg1813633
hg1713633
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524871
Supporting Variants
Samples
Known GenesSLCO3A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700876
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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