A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690587



Internal ID15427239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93608310..93688487hg38UCSC Ensembl
Innerchr15:94151539..94231716hg19UCSC Ensembl
Innerchr15:91952543..92032720hg18UCSC Ensembl
Innerchr15:91952543..92032720hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3880178
hg1980178
hg1880178
hg1780178
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)nssv690587
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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