A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528870



Internal ID15456163
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705550
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528870
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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