A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024660



Internal ID19113877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:26017331..26121415hg38UCSC Ensembl
Innerchr5:26017440..26121524hg19UCSC Ensembl
Innerchr5:26053197..26157281hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38104085
hg19104085
hg18104085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635960
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)nsv1024660
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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