A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528743



Internal ID15456036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116851586..117525430hg38UCSC Ensembl
Innerchr9:119613865..120287708hg19UCSC Ensembl
Innerchr9:118653686..119327529hg18UCSC Ensembl
Innerchr9:116693419..117367262hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38673845
hg19673844
hg18673844
hg17673844
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705403
Samples
Known GenesASTN2, SNORA70C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528743
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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