A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040555



Internal ID19129774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37801979..37845396hg38UCSC Ensembl
Innerchr14:38271184..38314601hg19UCSC Ensembl
Innerchr14:37340935..37384352hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3843418
hg1943418
hg1843418
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528632, nssv3528631
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)nsv1040555
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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