A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657914



Internal ID15394566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35301212..35452449hg38UCSC Ensembl
Innerchr16:34535583..34686820hg19UCSC Ensembl
Innerchr16:34393084..34544321hg18UCSC Ensembl
Innerchr16:34393084..34544321hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38151238
hg19151238
hg18151238
hg17151238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516385
Supporting Variants
Samples
Known GenesLOC283914
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657914
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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