A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946324



Internal ID18246488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148237136..148309631hg38UCSC Ensembl
Innerchr1:147709408..147781739hg19UCSC Ensembl
Innerchr1:146176032..146248363hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3872496
hg1972332
hg1872332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1794861, nssv1794854, nssv1794856, nssv1794862, nssv1794857, nssv1794858, nssv1794853, nssv1794855, nssv1794860, nssv1794859
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNBPF10, NBPF8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv946324
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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