A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526640



Internal ID15453933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29034432..29127579hg38UCSC Ensembl
Innerchr9:29034430..29127577hg19UCSC Ensembl
Innerchr9:29024430..29117577hg18UCSC Ensembl
Innerchr9:29024430..29117577hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3893148
hg1993148
hg1893148
hg1793148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702963
Samples
Known GenesLINGO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526640
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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