A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052588



Internal ID19141807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45284734..45534535hg38UCSC Ensembl
Innerchr14:45753937..46003738hg19UCSC Ensembl
Innerchr14:44823687..45073488hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38249802
hg19249802
hg18249802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1905n100
Supporting Variantsnssv3530445
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)nsv1052588
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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