A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945762



Internal ID18592613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8823310..8836744hg38UCSC Ensembl
Innerchr1:8883369..8896803hg19UCSC Ensembl
Innerchr1:8805956..8819390hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3813435
hg1913435
hg1813435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1752805, nssv1752807, nssv1752802, nssv1752809, nssv1752804, nssv1752808, nssv1752803, nssv1752801, nssv1752806, nssv1752810
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)nsv945762
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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