A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683536



Internal ID15420188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35126609..35526596hg38UCSC Ensembl
Innerchr16:34360980..34760967hg19UCSC Ensembl
Innerchr16:34218481..34618468hg18UCSC Ensembl
Innerchr16:34218481..34618468hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38399988
hg19399988
hg18399988
hg17399988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516385
Supporting Variants
Samples
Known GenesLOC100130700, LOC146481, LOC283914, UBE2MP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683536
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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