A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965739



Internal ID18600969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:63576522..63577140hg38UCSC Ensembl
Innerchr6:64286427..64287045hg19UCSC Ensembl
Innerchr6:64344386..64345004hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38619
hg19619
hg18619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2414295, nssv2414301, nssv2414292, nssv2414299, nssv2414300, nssv2414294, nssv2414296, nssv2414297, nssv2414293, nssv2414298
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPTP4A1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965739
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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