A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946919



Internal ID18247083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148554080..148554695hg38UCSC Ensembl
Innerchr1:148289102..148289717hg19UCSC Ensembl
Innerchr1:146655726..146656341hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38616
hg19616
hg18616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2595277, nssv2595284, nssv2595336, nssv2595341, nssv2595334, nssv2595276, nssv2595343, nssv2595285, nssv2595335, nssv2595279, nssv2595338, nssv2595342, nssv2595278, nssv2595339, nssv2595282, nssv2595283, nssv2595280, nssv2595340, nssv2595281, nssv2595337
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLOC101929780, NBPF10, NBPF14, NBPF8, NBPF9
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv946919
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer