A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696026



Internal ID15085992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13742024..13742515hg38UCSC Ensembl
Innerchr8:13599533..13600024hg19UCSC Ensembl
Innerchr8:13643904..13644395hg18UCSC Ensembl
Innerchr8:13643904..13644395hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38492
hg19492
hg18492
hg17492
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517019
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696026
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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