A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549165



Internal ID18847446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31960187..32169643hg38UCSC Ensembl
Innerchr16:31971508..32180964hg19UCSC Ensembl
Innerchr16:31879009..32088465hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38209457
hg19209457
hg18209457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055504
Supporting Variants
Samples
Known GenesHERC2P4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3549165
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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