A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524744



Internal ID15105351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109955225..110158061hg38UCSC Ensembl
Innerchr9:112717505..112920341hg19UCSC Ensembl
Innerchr9:111757326..111960162hg18UCSC Ensembl
Innerchr9:109797060..109999896hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38202837
hg19202837
hg18202837
hg17202837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv494n21
Supporting Variantsnssv700735
Samples
Known GenesAKAP2, PALM2-AKAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524744
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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