A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042236



Internal ID19131455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42489030..42644771hg38UCSC Ensembl
Innerchr14:42958233..43113974hg19UCSC Ensembl
Innerchr14:42027983..42183724hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38155742
hg19155742
hg18155742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1888n100
Supporting Variantsnssv3712300
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)nsv1042236
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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