A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966332



Internal ID18601562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:159025576..159027235hg38UCSC Ensembl
Innerchr4:159946728..159948387hg19UCSC Ensembl
Innerchr4:160166178..160167837hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381660
hg191660
hg181660
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2339403, nssv2339404, nssv2339398, nssv2339397, nssv2339400, nssv2339399, nssv2339396, nssv2339402, nssv2339395, nssv2339401
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC4orf45
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966332
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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