A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965674



Internal ID18600904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1513101..1514435hg38UCSC Ensembl
Innerchr6:1513336..1514670hg19UCSC Ensembl
Innerchr6:1458335..1459669hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381335
hg191335
hg181335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2391822, nssv2391820, nssv2391817, nssv2391814, nssv2391821, nssv2391815, nssv2391819, nssv2391823, nssv2391816, nssv2391818
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)nsv965674
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