A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021139



Internal ID18763673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115701027..115795583hg38UCSC Ensembl
Innerchr5:115036724..115131280hg19UCSC Ensembl
Innerchr5:115064623..115159179hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3894557
hg1994557
hg1894557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5788n100
Supporting Variantsnssv3647086
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)nsv1021139
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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