A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038437



Internal ID19127656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43357427..43765759hg38UCSC Ensembl
Innerchr14:43826630..44234962hg19UCSC Ensembl
Innerchr14:42896380..43304712hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38408333
hg19408333
hg18408333
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1890n100
Supporting Variantsnssv3530237
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)nsv1038437
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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