A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693331



Internal ID15083297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10386989..10459815hg38UCSC Ensembl
Innerchr16:10480846..10553672hg19UCSC Ensembl
Innerchr16:10388347..10461173hg18UCSC Ensembl
Innerchr16:10388347..10461173hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3872827
hg1972827
hg1872827
hg1772827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519263
Supporting Variants
Samples
Known GenesATF7IP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693331
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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