A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960261



Internal ID18595514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14669635..14709749hg38UCSC Ensembl
Innerchr18:14669634..14709748hg19UCSC Ensembl
Innerchr18:14659634..14699748hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3840115
hg1940115
hg1840115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2117682, nssv2117675, nssv2117680, nssv2117673, nssv2117677, nssv2117678, nssv2117681, nssv2117676, nssv2117679, nssv2117674
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)nsv960261
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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