A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038781



Internal ID19128000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42637857..42849027hg38UCSC Ensembl
Innerchr14:43107060..43318230hg19UCSC Ensembl
Innerchr14:42176810..42387980hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38211171
hg19211171
hg18211171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712303
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)nsv1038781
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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