A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526470



Internal ID15453763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103325070..103339726hg38UCSC Ensembl
Innerchr9:106087352..106102008hg19UCSC Ensembl
Innerchr9:105127173..105141829hg18UCSC Ensembl
Innerchr9:103166907..103181563hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3814657
hg1914657
hg1814657
hg1714657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702774
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526470
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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