A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964108



Internal ID18599346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164377435..164380227hg38UCSC Ensembl
Innerchr4:165298587..165301379hg19UCSC Ensembl
Innerchr4:165518037..165520829hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382793
hg192793
hg182793
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2339295, nssv2339299, nssv2339302, nssv2339301, nssv2339303, nssv2339297, nssv2339296, nssv2339294, nssv2339300, nssv2339298
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMARCH1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964108
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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