A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526321



Internal ID15453614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:63931254..63934853hg38UCSC Ensembl
Innerchr8:64843811..64847410hg19UCSC Ensembl
Innerchr8:65006365..65009964hg18UCSC Ensembl
Innerchr8:65006365..65009964hg17UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg383600
hg193600
hg183600
hg173600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702609
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526321
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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