A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946096



Internal ID18592946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:100585968..100589993hg38UCSC Ensembl
Innerchr1:101051524..101055549hg19UCSC Ensembl
Innerchr1:100824112..100828137hg18UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg384026
hg194026
hg184026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1778041, nssv1778040, nssv1778037, nssv1778045, nssv1778042, nssv1778043, nssv1778044, nssv1778036, nssv1778039, nssv1778038
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)nsv946096
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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