A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524474



Internal ID15451767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19430333..19583439hg38UCSC Ensembl
Innerchr9:19430331..19583437hg19UCSC Ensembl
Innerchr9:19420331..19573437hg18UCSC Ensembl
Innerchr9:19420331..19573437hg17UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38153107
hg19153107
hg18153107
hg17153107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700412
Samples
Known GenesACER2, SLC24A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524474
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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