A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519332



Internal ID15446625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34784171..34819534hg38UCSC Ensembl
Innerchr9:34784168..34819531hg19UCSC Ensembl
Innerchr9:34774168..34809531hg18UCSC Ensembl
Innerchr9:34774168..34809531hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3835364
hg1935364
hg1835364
hg1735364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696797
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519332
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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