A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965163



Internal ID18253711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46023399..46026438hg38UCSC Ensembl
Innerchr3:46064891..46067930hg19UCSC Ensembl
Innerchr3:46039895..46042934hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383040
hg193040
hg183040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2281129, nssv2281136, nssv2281134, nssv2281132, nssv2281135, nssv2281127, nssv2281130, nssv2281133, nssv2281131, nssv2281128
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesXCR1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965163
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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