A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684252



Internal ID15420904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35234530..35526596hg38UCSC Ensembl
Innerchr16:34468901..34760967hg19UCSC Ensembl
Innerchr16:34326402..34618468hg18UCSC Ensembl
Innerchr16:34326402..34618468hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38292067
hg19292067
hg18292067
hg17292067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516385
Supporting Variants
Samples
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684252
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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