A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946026



Internal ID18592876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:83132401..83164708hg38UCSC Ensembl
Innerchr1:83598084..83630391hg19UCSC Ensembl
Innerchr1:83370672..83402979hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3832308
hg1932308
hg1832308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1773094, nssv1773095, nssv1773090, nssv1773089, nssv1773091, nssv1773087, nssv1773093, nssv1773092, nssv1773088, nssv1773096
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)nsv946026
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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