A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021109



Internal ID19110327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17601432..17770843hg38UCSC Ensembl
Innerchr5:17601541..17770952hg19UCSC Ensembl
Innerchr5:17644644..17806713hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38169412
hg19169412
hg18162070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5589n100
Supporting Variantsnssv3745823
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)nsv1021109
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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