A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967023



Internal ID18602252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:73919573..73922130hg38UCSC Ensembl
Innerchr3:73968724..73971281hg19UCSC Ensembl
Innerchr3:74051414..74053971hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382558
hg192558
hg182558
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2285436, nssv2285437, nssv2285445, nssv2285443, nssv2285439, nssv2285442, nssv2285438, nssv2285444, nssv2285441, nssv2285440
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)nsv967023
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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