A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974371



Internal ID18609582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100481053..100482999hg38UCSC Ensembl
Innerchr14:100947390..100949336hg19UCSC Ensembl
Innerchr14:100017143..100019089hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381947
hg191947
hg181947
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1998071, nssv1998070, nssv1998074, nssv1998068, nssv1998067, nssv1998075, nssv1998069, nssv1998076, nssv1998073, nssv1998072
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesWDR25
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974371
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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