A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519263



Internal ID15099870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10386989..10466528hg38UCSC Ensembl
Innerchr16:10480846..10560385hg19UCSC Ensembl
Innerchr16:10388347..10467886hg18UCSC Ensembl
Innerchr16:10388347..10467886hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3879540
hg1979540
hg1879540
hg1779540
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686261, nssv663542, nssv655115, nssv693331, nssv692779
Samples
Known GenesATF7IP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519263
Frequency
Sample Size2026
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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