A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981459



Internal ID18616656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39865804..39866778hg38UCSC Ensembl
Innerchr7:39905403..39906377hg19UCSC Ensembl
Innerchr7:39871928..39872902hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38975
hg19975
hg18975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2445768, nssv2445766, nssv2445765, nssv2445772, nssv2445769, nssv2445770, nssv2445771, nssv2445764, nssv2445767, nssv2445763
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)nsv981459
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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