A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524264



Internal ID15451557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16596073..16611694hg38UCSC Ensembl
Innerchr9:16596071..16611692hg19UCSC Ensembl
Innerchr9:16586071..16601692hg18UCSC Ensembl
Innerchr9:16586071..16601692hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3815622
hg1915622
hg1815622
hg1715622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700161
Samples
Known GenesBNC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524264
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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