A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052135



Internal ID19141354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66207866..66376408hg38UCSC Ensembl
Innerchr14:66674584..66843126hg19UCSC Ensembl
Innerchr14:65744337..65912879hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38168543
hg19168543
hg18168543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531085
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)nsv1052135
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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