A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665108



Internal ID15401760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127513023..127519628hg38UCSC Ensembl
Innerchr8:128525268..128531873hg19UCSC Ensembl
Innerchr8:128594450..128601055hg18UCSC Ensembl
Innerchr8:128594450..128601055hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg386606
hg196606
hg186606
hg176606
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517444
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665108
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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