A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023123



Internal ID19112340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12488191..12686504hg38UCSC Ensembl
Innerchr5:12488303..12686616hg19UCSC Ensembl
Innerchr5:12541303..12739616hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38198314
hg19198314
hg18198314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5571n100
Supporting Variantsnssv3638209
Samples
Known GenesCT49
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023123
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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