A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966347



Internal ID18601577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184569583..184584524hg38UCSC Ensembl
Innerchr4:185490737..185505678hg19UCSC Ensembl
Innerchr4:185727731..185742672hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3814942
hg1914942
hg1814942
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2343455, nssv2343454, nssv2343449, nssv2343451, nssv2343453, nssv2343452, nssv2343457, nssv2343450, nssv2343456, nssv2343458
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)nsv966347
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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