A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047105



Internal ID19136324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20880514..20941810hg38UCSC Ensembl
Innerchr14:21348673..21409969hg19UCSC Ensembl
Innerchr14:20418513..20479809hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3861297
hg1961297
hg1861297
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1798n100
Supporting Variantsnssv3712138, nssv3530737, nssv3530744, nssv3712134, nssv3530743, nssv3530747, nssv3530746, nssv3530738, nssv3712135, nssv3712136, nssv3530740, nssv3530739, nssv3530745, nssv3530741, nssv3712137, nssv3530742
Samples
Known GenesECRP, RNASE3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047105
Frequency
Sample Size11257
Observed Gain10
Observed Loss6
Observed Complex0
Frequencyn/a


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