A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660509



Internal ID15397161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87287299..87320484hg38UCSC Ensembl
Innerchr15:87830530..87863715hg19UCSC Ensembl
Innerchr15:85631534..85664719hg18UCSC Ensembl
Innerchr15:85631534..85664719hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3833186
hg1933186
hg1833186
hg1733186
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517389
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660509
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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