A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965227



Internal ID18600461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158275336..158276445hg38UCSC Ensembl
Innerchr3:157993125..157994234hg19UCSC Ensembl
Innerchr3:159475819..159476928hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg381110
hg191110
hg181110
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2302245, nssv2302242, nssv2302247, nssv2302243, nssv2302244, nssv2302241, nssv2302239, nssv2302246, nssv2302248, nssv2302240
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRSRC1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965227
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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