A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960649



Internal ID18595896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10614547..10659614hg38UCSC Ensembl
Innerchr18:10614544..10659611hg19UCSC Ensembl
Innerchr18:10604544..10649611hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3845068
hg1945068
hg1845068
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2114924, nssv2114923, nssv2114926, nssv2114925, nssv2114927, nssv2114920, nssv2114928, nssv2114929, nssv2114922, nssv2114921
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)nsv960649
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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