A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964102



Internal ID18599340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148526448..148527539hg38UCSC Ensembl
Innerchr4:149447600..149448691hg19UCSC Ensembl
Innerchr4:149667050..149668141hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381092
hg191092
hg181092
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2338115, nssv2338116, nssv2338117, nssv2338113, nssv2338118, nssv2338114, nssv2338119, nssv2338111, nssv2338112, nssv2338120
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)nsv964102
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