A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967089



Internal ID18602318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:169709438..169715778hg38UCSC Ensembl
Innerchr3:169427226..169433566hg19UCSC Ensembl
Innerchr3:170909920..170916260hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg386341
hg196341
hg186341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2304839, nssv2304843, nssv2304844, nssv2304838, nssv2304840, nssv2304845, nssv2304841, nssv2304842, nssv2304847, nssv2304846
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)nsv967089
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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