A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945706



Internal ID18592557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:125400..176984hg38UCSC Ensembl
Innerchr1:125400..176984hg19UCSC Ensembl
Innerchr1:115263..166847hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3851585
hg1951585
hg1851585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1751892, nssv1751890, nssv1751894, nssv1751900, nssv1751891, nssv1751896, nssv1751889, nssv1751897, nssv1751895, nssv1751893
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC729737
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945706
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