A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966783



Internal ID18602013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39873693..39884059hg38UCSC Ensembl
Innerchr7:39913292..39923658hg19UCSC Ensembl
Innerchr7:39879817..39890183hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3810367
hg1910367
hg1810367
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2444099, nssv2444107, nssv2444104, nssv2444102, nssv2444900, nssv2444105, nssv2444103, nssv2444100, nssv2444106, nssv2444101
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)nsv966783
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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