A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963209



Internal ID18598450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:7349801..7350301hg38UCSC Ensembl
Innerchr2:7489932..7490432hg19UCSC Ensembl
Innerchr2:7407383..7407883hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2163513, nssv2163517, nssv2163511, nssv2163512, nssv2163519, nssv2163518, nssv2163514, nssv2163516, nssv2163520, nssv2163515
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)nsv963209
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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