A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974325



Internal ID18609536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35889311..35892746hg38UCSC Ensembl
Innerchr14:36358517..36361952hg19UCSC Ensembl
Innerchr14:35428268..35431703hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg383436
hg193436
hg183436
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1982751, nssv1982749, nssv1982750, nssv1982758, nssv1982755, nssv1982752, nssv1982757, nssv1982753, nssv1982754, nssv1982756
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)nsv974325
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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