A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981439



Internal ID18616636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:22881031..22885050hg38UCSC Ensembl
Innerchr7:22920650..22924669hg19UCSC Ensembl
Innerchr7:22887175..22891194hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384020
hg194020
hg184020
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2436781, nssv2436789, nssv2436788, nssv2436785, nssv2436783, nssv2436784, nssv2436782, nssv2436787, nssv2436786, nssv2436780
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)nsv981439
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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