A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522210



Internal ID15102817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40864809..40936014hg38UCSC Ensembl
Innerchr8:40722328..40793533hg19UCSC Ensembl
Innerchr8:40841485..40912690hg18UCSC Ensembl
Innerchr8:40841485..40912690hg17UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3871206
hg1971206
hg1871206
hg1771206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694986
Samples
Known GenesZMAT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522210
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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