A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960266



Internal ID18595519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14984975..14987576hg38UCSC Ensembl
Innerchr18:14984974..14987575hg19UCSC Ensembl
Innerchr18:14974974..14977575hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382602
hg192602
hg182602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2658483, nssv2658480, nssv2658488, nssv2658485, nssv2658487, nssv2658481, nssv2658484, nssv2658482, nssv2658489, nssv2658486
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)nsv960266
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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