A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1981685



Internal ID17732996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28265159..28265772hg38UCSC Ensembl
Innerchr14:28734365..28734978hg19UCSC Ensembl
Innerchr14:27804116..27804729hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38614
hg19614
hg18614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv977449
Supporting Variants
SamplesHGDP00456
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1981685
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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