A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977450



Internal ID18612656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28673070..28673681hg38UCSC Ensembl
Innerchr14:29142276..29142887hg19UCSC Ensembl
Innerchr14:28212027..28212638hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38612
hg19612
hg18612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1981720, nssv1981716, nssv1981713, nssv1981721, nssv1981714, nssv1981719, nssv1981718, nssv1981715, nssv1981717, nssv1981722
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)nsv977450
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer