A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946041



Internal ID18592891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:86778669..86789258hg38UCSC Ensembl
Innerchr1:87244352..87254941hg19UCSC Ensembl
Innerchr1:87016940..87027529hg18UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3810590
hg1910590
hg1810590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1774939, nssv1774943, nssv1774938, nssv1774940, nssv1774942, nssv1774945, nssv1774944, nssv1774946, nssv1774941, nssv1774947
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)nsv946041
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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