A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663542



Internal ID15053508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10386989..10437453hg38UCSC Ensembl
Innerchr16:10480846..10531310hg19UCSC Ensembl
Innerchr16:10388347..10438811hg18UCSC Ensembl
Innerchr16:10388347..10438811hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3850465
hg1950465
hg1850465
hg1750465
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)nssv663542
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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