A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528823



Internal ID15456116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114284841..114346385hg38UCSC Ensembl
Innerchr9:117047121..117108665hg19UCSC Ensembl
Innerchr9:116086942..116148486hg18UCSC Ensembl
Innerchr9:114126675..114188219hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3861545
hg1961545
hg1861545
hg1761545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705497
Samples
Known GenesAKNA, COL27A1, ORM1, ORM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528823
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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