A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698565



Internal ID15435217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46359028..46426613hg38UCSC Ensembl
Innerchr8:47270650..47338235hg19UCSC Ensembl
Innerchr8:47389815..47457400hg18UCSC Ensembl
Innerchr8:47389815..47457400hg17UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3867586
hg1967586
hg1867586
hg1767586
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698565
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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