A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029772



Internal ID19118991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:86107012..86152786hg38UCSC Ensembl
Innerchr5:85402830..85448604hg19UCSC Ensembl
Innerchr5:85438586..85484360hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3845775
hg1945775
hg1845775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5713n100
Supporting Variantsnssv3639177
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029772
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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