A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521643



Internal ID15448936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:125997798..126006571hg38UCSC Ensembl
Innerchr8:127010042..127018815hg19UCSC Ensembl
Innerchr8:127079224..127087997hg18UCSC Ensembl
Innerchr8:127079224..127087997hg17UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg388774
hg198774
hg188774
hg178774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698263
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521643
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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