A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525916



Internal ID15453209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:80598186..80606085hg38UCSC Ensembl
Innerchr8:81510421..81518320hg19UCSC Ensembl
Innerchr8:81672976..81680875hg18UCSC Ensembl
Innerchr8:81672976..81680875hg17UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg387900
hg197900
hg187900
hg177900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702120
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525916
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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