A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058634



Internal ID19147853
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 StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3556156
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)nsv1058634
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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