A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946156



Internal ID18593006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:114534852..114538267hg38UCSC Ensembl
Innerchr1:115077473..115080888hg19UCSC Ensembl
Innerchr1:114878996..114882411hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg383416
hg193416
hg183416
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1783981, nssv1783982, nssv1783978, nssv1783977, nssv1783975, nssv1783980, nssv1783976, nssv1783973, nssv1783974, nssv1783979
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)nsv946156
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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