A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945715



Internal ID18592566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:383955..447598hg38UCSC Ensembl
Innerchr1:371739..435382hg19UCSC Ensembl
Innerchr1:361602..425245hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3863644
hg1963644
hg1863644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1756514, nssv1756508, nssv1756509, nssv1756515, nssv1756511, nssv1756513, nssv1756510, nssv1756517, nssv1756516, nssv1756512
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)nsv945715
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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