A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981514



Internal ID18270025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66845152..66901253hg38UCSC Ensembl
Innerchr7:66310139..66366240hg19UCSC Ensembl
Innerchr7:65947574..66003675hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3856102
hg1956102
hg1856102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2460636, nssv2460635, nssv2460634, nssv2460641, nssv2460637, nssv2460638, nssv2460642, nssv2460633, nssv2460639, nssv2460640
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)nsv981514
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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