A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967772



Internal ID18603000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87891897..87894115hg38UCSC Ensembl
Innerchr4:88813049..88815267hg19UCSC Ensembl
Innerchr4:89032073..89034291hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382219
hg192219
hg182219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2328117, nssv2328121, nssv2328119, nssv2328120, nssv2328115, nssv2328124, nssv2328122, nssv2328116, nssv2328118, nssv2328123
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)nsv967772
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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