A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979136



Internal ID18267653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:151801527..151803208hg38UCSC Ensembl
Innerchr2:152658041..152659722hg19UCSC Ensembl
Innerchr2:152366287..152367968hg18UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg381682
hg191682
hg181682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2207033, nssv2207038, nssv2207036, nssv2207040, nssv2207037, nssv2207039, nssv2207032, nssv2207034, nssv2207041, nssv2207035
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesARL5A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979136
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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