A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945299



Internal ID18592150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:220314480..220318275hg38UCSC Ensembl
Innerchr1:220487822..220491617hg19UCSC Ensembl
Innerchr1:218554445..218558240hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383796
hg193796
hg183796
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1818922, nssv1818926, nssv1818927, nssv1818925, nssv1818921, nssv1818919, nssv1818924, nssv1818923, nssv1818920, nssv1818928
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)nsv945299
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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