A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966308



Internal ID18601538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:110398772..110400423hg38UCSC Ensembl
Innerchr4:111319928..111321579hg19UCSC Ensembl
Innerchr4:111539377..111541028hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381652
hg191652
hg181652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2332121, nssv2332124, nssv2332122, nssv2332128, nssv2332123, nssv2332127, nssv2332120, nssv2332125, nssv2332126, nssv2332129
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)nsv966308
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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