A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966877



Internal ID18602106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111971212..111972212hg38UCSC Ensembl
Innerchr7:111611267..111612267hg19UCSC Ensembl
Innerchr7:111398503..111399503hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2475339, nssv2475342, nssv2475338, nssv2475344, nssv2475340, nssv2475343, nssv2475345, nssv2475341, nssv2475336, nssv2475337
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDOCK4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966877
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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