A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042258



Internal ID19131477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45867189..45984547hg38UCSC Ensembl
Innerchr14:46336392..46453750hg19UCSC Ensembl
Innerchr14:45406142..45523500hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38117359
hg19117359
hg18117359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531635
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)nsv1042258
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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