A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960268



Internal ID18595521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15381175..15410899hg38UCSC Ensembl
Innerchr18:15381174..15410898hg19UCSC Ensembl
Innerchr18:15371174..15401221hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg3829725
hg1929725
hg1830048
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2120770, nssv2120769, nssv2120775, nssv2120777, nssv2120772, nssv2120771, nssv2120773, nssv2120776, nssv2120778, nssv2120774
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960268
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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