A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974327



Internal ID18609538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36371370..36372688hg38UCSC Ensembl
Innerchr14:36840575..36841893hg19UCSC Ensembl
Innerchr14:35910326..35911644hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg381319
hg191319
hg181319
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1983741, nssv1983737, nssv1983744, nssv1983743, nssv1983736, nssv1983739, nssv1983738, nssv1983735, nssv1983742, nssv1983740
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974327
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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