A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969398



Internal ID18604625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:48211923..48214185hg38UCSC Ensembl
Innerchr6:48179659..48181921hg19UCSC Ensembl
Innerchr6:48287618..48289880hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg382263
hg192263
hg182263
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2407889, nssv2407890, nssv2407883, nssv2407888, nssv2407886, nssv2407884, nssv2407891, nssv2407885, nssv2407887, nssv2407882
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)nsv969398
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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