A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527071



Internal ID15107678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:100573021..100583678hg38UCSC Ensembl
Innerchr8:101585249..101595906hg19UCSC Ensembl
Innerchr8:101654425..101665082hg18UCSC Ensembl
Innerchr8:101654425..101665082hg17UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3810658
hg1910658
hg1810658
hg1710658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703450
Samples
Known GenesSNX31
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527071
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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