A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960681



Internal ID18595928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15228131..15252227hg38UCSC Ensembl
Innerchr18:15228130..15252226hg19UCSC Ensembl
Innerchr18:15218130..15242226hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3824097
hg1924097
hg1824097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2662142, nssv2662145, nssv2662139, nssv2662148, nssv2662144, nssv2662141, nssv2662147, nssv2662146, nssv2662140, nssv2662143
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960681
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer