A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705550



Internal ID15442202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:126369101..126373949hg38UCSC Ensembl
Innerchr8:127381346..127386194hg19UCSC Ensembl
Innerchr8:127450528..127455376hg18UCSC Ensembl
Innerchr8:127450528..127455376hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg384849
hg194849
hg184849
hg174849
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528870
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705550
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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