A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945875



Internal ID18592725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:33501159..33502205hg38UCSC Ensembl
Innerchr1:33966759..33967805hg19UCSC Ensembl
Innerchr1:33739346..33740392hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381047
hg191047
hg181047
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1759303, nssv1759306, nssv1759300, nssv1759305, nssv1759304, nssv1759298, nssv1759301, nssv1759302, nssv1759299, nssv1759307
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)nsv945875
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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