A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966328



Internal ID18601558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152549012..152558159hg38UCSC Ensembl
Innerchr4:153470164..153479311hg19UCSC Ensembl
Innerchr4:153689614..153698761hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg389148
hg199148
hg189148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2336928, nssv2336933, nssv2336934, nssv2336929, nssv2336932, nssv2336926, nssv2336930, nssv2336927, nssv2336935, nssv2336931
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)nsv966328
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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