A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526931



Internal ID15107538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8907655..8909371hg38UCSC Ensembl
Innerchr8:8765165..8766881hg19UCSC Ensembl
Innerchr8:8802575..8804291hg18UCSC Ensembl
Innerchr8:8802575..8804291hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381717
hg191717
hg181717
hg171717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703298
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526931
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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