A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024307



Internal ID19113524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28936088..29145569hg38UCSC Ensembl
Innerchr5:28936195..29145676hg19UCSC Ensembl
Innerchr5:28971952..29181433hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38209482
hg19209482
hg18209482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5613n100
Supporting Variantsnssv3635979
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)nsv1024307
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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