A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981472



Internal ID18616669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55645783..55646880hg38UCSC Ensembl
Innerchr7:55713476..55714573hg19UCSC Ensembl
Innerchr7:55680970..55682067hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg381098
hg191098
hg181098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2446836, nssv2446838, nssv2446840, nssv2446841, nssv2446837, nssv2446835, nssv2446839, nssv2446834, nssv2446842, nssv2446843
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)nsv981472
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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