A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515562



Internal ID15096169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110157886..110175898hg38UCSC Ensembl
Innerchr9:112920166..112938178hg19UCSC Ensembl
Innerchr9:111959987..111977999hg18UCSC Ensembl
Innerchr9:109999721..110017733hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3818013
hg1918013
hg1818013
hg1718013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657331, nssv663915, nssv681426, nssv659585
Samples
Known GenesAKAP2, PALM2-AKAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515562
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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