A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556156



Internal ID18854437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35232188..35504875hg38UCSC Ensembl
Innerchr16:34466559..34739246hg19UCSC Ensembl
Innerchr16:34324060..34596747hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38272688
hg19272688
hg18272688
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058634
Supporting Variants
Samples
Known GenesLOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3556156
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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