A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965782



Internal ID18601012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160730072..160731316hg38UCSC Ensembl
Innerchr6:161151104..161152348hg19UCSC Ensembl
Innerchr6:161071094..161072338hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381245
hg191245
hg181245
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2430602, nssv2430601, nssv2430607, nssv2430610, nssv2430609, nssv2430606, nssv2430603, nssv2430608, nssv2430605, nssv2430604
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPLG
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965782
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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