A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967791



Internal ID18603019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:119395437..119402291hg38UCSC Ensembl
Innerchr4:120316592..120323446hg19UCSC Ensembl
Innerchr4:120536040..120542894hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg386855
hg196855
hg186855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2333786, nssv2333788, nssv2333787, nssv2333790, nssv2333792, nssv2333791, nssv2333789, nssv2333785, nssv2333784, nssv2333783
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)nsv967791
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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