A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020870



Internal ID19110088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114592587..114644459hg38UCSC Ensembl
Innerchr5:113928284..113980156hg19UCSC Ensembl
Innerchr5:113956183..114008055hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3851873
hg1951873
hg1851873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5785n100
Supporting Variantsnssv3647074
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)nsv1020870
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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