A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019614



Internal ID19108832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20916471..21068126hg38UCSC Ensembl
Innerchr5:20916580..21068235hg19UCSC Ensembl
Innerchr5:20952337..21103992hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38151656
hg19151656
hg18151656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745836, nssv3635923
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)nsv1019614
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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