A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041159



Internal ID19130378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43354078..43765759hg38UCSC Ensembl
Innerchr14:43823281..44234962hg19UCSC Ensembl
Innerchr14:42893031..43304712hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38411682
hg19411682
hg18411682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1890n100
Supporting Variantsnssv3530232, nssv3712305, nssv3530230, nssv3530231
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)nsv1041159
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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