A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656004



Internal ID15392656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85178426..85185603hg38UCSC Ensembl
Innerchr15:85721657..85728834hg19UCSC Ensembl
Innerchr15:83522661..83529838hg18UCSC Ensembl
Innerchr15:83522661..83529838hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg387178
hg197178
hg187178
hg177178
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517561
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656004
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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