A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039187



Internal ID19128406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2593295..2676863hg38UCSC Ensembl
Innerchr16:2643296..2726864hg19UCSC Ensembl
Innerchr16:2583297..2666865hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3883569
hg1983569
hg1883569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2693n100
Supporting Variantsnssv3718832
Samples
Known GenesERVK13-1, FLJ42627, LOC652276, PDPK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039187
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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