A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969353



Internal ID18257894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24976542..24977812hg38UCSC Ensembl
Innerchr6:24976770..24978040hg19UCSC Ensembl
Innerchr6:25084749..25086019hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg381271
hg191271
hg181271
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2394897, nssv2394899, nssv2394891, nssv2394895, nssv2394894, nssv2394896, nssv2394893, nssv2394892, nssv2395428, nssv2394898
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFAM65B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969353
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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