A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966865



Internal ID18255408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100137962..100142855hg38UCSC Ensembl
Innerchr7:99735585..99740478hg19UCSC Ensembl
Innerchr7:99573521..99578414hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg384894
hg194894
hg184894
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2471463, nssv2471464, nssv2471467, nssv2472261, nssv2472260, nssv2471466, nssv2471462, nssv2471465, nssv2471460, nssv2471461
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)nsv966865
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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