A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028664



Internal ID19117882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116265825..116295181hg38UCSC Ensembl
Innerchr5:115601522..115630878hg19UCSC Ensembl
Innerchr5:115629421..115658777hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3829357
hg1929357
hg1829357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5792n100
Supporting Variantsnssv3647208
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)nsv1028664
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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