A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945871



Internal ID18592721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32411992..32430496hg38UCSC Ensembl
Innerchr1:32877593..32896097hg19UCSC Ensembl
Innerchr1:32650180..32668684hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3818505
hg1918505
hg1818505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1758301, nssv1758295, nssv1758298, nssv1758303, nssv1758302, nssv1758297, nssv1758299, nssv1758294, nssv1758300, nssv1758296
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)nsv945871
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