A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945820



Internal ID18592670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22320773..22324126hg38UCSC Ensembl
Innerchr1:22647266..22650619hg19UCSC Ensembl
Innerchr1:22519853..22523206hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg383354
hg193354
hg183354
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1765053, nssv1765057, nssv1765051, nssv1765059, nssv1765050, nssv1765055, nssv1765052, nssv1765058, nssv1765056, nssv1765054
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)nsv945820
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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