A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945886



Internal ID18592736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38709552..38712385hg38UCSC Ensembl
Innerchr1:39175224..39178057hg19UCSC Ensembl
Innerchr1:38947811..38950644hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382834
hg192834
hg182834
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1760338, nssv1760334, nssv1760343, nssv1760335, nssv1760337, nssv1760342, nssv1760336, nssv1760341, nssv1760339, nssv1760340
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)nsv945886
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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