A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966303



Internal ID18601533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102728072..102732286hg38UCSC Ensembl
Innerchr4:103649229..103653443hg19UCSC Ensembl
Innerchr4:103868273..103872486hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg384215
hg194215
hg184214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2329591, nssv2329584, nssv2329586, nssv2329588, nssv2329593, nssv2329590, nssv2329589, nssv2329587, nssv2329585, nssv2329592
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMANBA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966303
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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