A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966763



Internal ID18601993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23480761..23482480hg38UCSC Ensembl
Innerchr7:23520380..23522099hg19UCSC Ensembl
Innerchr7:23486905..23488624hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381720
hg191720
hg181720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2438761, nssv2438752, nssv2438754, nssv2438760, nssv2438757, nssv2438756, nssv2438753, nssv2438758, nssv2438755, nssv2438759
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)nsv966763
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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