A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978606



Internal ID18613809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:12225801..12230994hg38UCSC Ensembl
Innerchr18:12225800..12230993hg19UCSC Ensembl
Innerchr18:12215800..12220993hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg385194
hg195194
hg185194
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2115765, nssv2115764, nssv2115771, nssv2115770, nssv2115768, nssv2115769, nssv2115766, nssv2115767, nssv2115762, nssv2115763
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)nsv978606
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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