A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945763



Internal ID18592614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8893567..8903950hg38UCSC Ensembl
Innerchr1:8953626..8964009hg19UCSC Ensembl
Innerchr1:8876213..8886596hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3810384
hg1910384
hg1810384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1753293, nssv1753290, nssv1753296, nssv1753295, nssv1753297, nssv1753298, nssv1753292, nssv1753294, nssv1753289, nssv1753291
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)nsv945763
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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