A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020655



Internal ID19109874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120394106..120446067hg38UCSC Ensembl
Innerchr5:119729801..119781762hg19UCSC Ensembl
Innerchr5:119757700..119809661hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3851962
hg1951962
hg1851962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746601
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)nsv1020655
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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