A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705214



Internal ID15441866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:135369352..135392641hg38UCSC Ensembl
Innerchr8:136381595..136404884hg19UCSC Ensembl
Innerchr8:136450777..136474066hg18UCSC Ensembl
Innerchr8:136450777..136474066hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3823290
hg1923290
hg1823290
hg1723290
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528589
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705214
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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