A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680403



Internal ID15070369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13742589..13751254hg38UCSC Ensembl
Innerchr8:13600098..13608763hg19UCSC Ensembl
Innerchr8:13644469..13653134hg18UCSC Ensembl
Innerchr8:13644469..13653134hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg388666
hg198666
hg188666
hg178666
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)nssv680403
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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