A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015280



Internal ID19104497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120828113..120971153hg38UCSC Ensembl
Innerchr5:120163808..120306848hg19UCSC Ensembl
Innerchr5:120191707..120334747hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38143041
hg19143041
hg18143041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5801n100
Supporting Variantsnssv3647996
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)nsv1015280
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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