A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043813



Internal ID19133032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41376753..41535992hg38UCSC Ensembl
Innerchr14:41845956..42005195hg19UCSC Ensembl
Innerchr14:40915706..41074945hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38159240
hg19159240
hg18159240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1884n100
Supporting Variantsnssv3712296
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)nsv1043813
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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