A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680238



Internal ID15416890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93608527..93691092hg38UCSC Ensembl
Innerchr15:94151756..94234321hg19UCSC Ensembl
Innerchr15:91952760..92035325hg18UCSC Ensembl
Innerchr15:91952760..92035325hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3882566
hg1982566
hg1882566
hg1782566
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515866
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680238
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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