A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024670



Internal ID19113887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116204889..116279762hg38UCSC Ensembl
Innerchr5:115540586..115615459hg19UCSC Ensembl
Innerchr5:115568485..115643358hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3874874
hg1974874
hg1874874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5791n100
Supporting Variantsnssv3647107
Samples
Known GenesCOMMD10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024670
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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