A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705771



Internal ID15442423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26148055..26157454hg38UCSC Ensembl
Innerchr15:26393202..26402601hg19UCSC Ensembl
Innerchr15:23944295..23953694hg18UCSC Ensembl
Innerchr15:23944295..23953694hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg389400
hg199400
hg189400
hg179400
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522418
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705771
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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