A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528964



Internal ID15109571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15760824..15875164hg38UCSC Ensembl
Innerchr9:15760822..15875162hg19UCSC Ensembl
Innerchr9:15750822..15865162hg18UCSC Ensembl
Innerchr9:15750822..15865162hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38114341
hg19114341
hg18114341
hg17114341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705661
Samples
Known GenesCCDC171
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528964
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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