A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965768



Internal ID18600998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:134897357..134898925hg38UCSC Ensembl
Innerchr6:135218495..135220063hg19UCSC Ensembl
Innerchr6:135260188..135261756hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381569
hg191569
hg181569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2424688, nssv2424686, nssv2424683, nssv2424687, nssv2424682, nssv2424680, nssv2424684, nssv2424689, nssv2424681, nssv2424685
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)nsv965768
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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