A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970078



Internal ID18605302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15845809..15849405hg38UCSC Ensembl
Innerchr6:15846040..15849636hg19UCSC Ensembl
Innerchr6:15954019..15957615hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383597
hg193597
hg183597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2394220, nssv2394213, nssv2394217, nssv2394212, nssv2394218, nssv2394214, nssv2394211, nssv2394216, nssv2394219, nssv2394215
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)nsv970078
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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