A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965773



Internal ID18601003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137543767..137544267hg38UCSC Ensembl
Innerchr6:137864904..137865404hg19UCSC Ensembl
Innerchr6:137906597..137907097hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2425209, nssv2425215, nssv2425216, nssv2425210, nssv2425212, nssv2425211, nssv2425207, nssv2425213, nssv2425208, nssv2425214
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)nsv965773
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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