A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981104



Internal ID18616303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10365076..10366572hg38UCSC Ensembl
Innerchr6:10365309..10366805hg19UCSC Ensembl
Innerchr6:10473295..10474791hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg381497
hg191497
hg181497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2393614, nssv2393621, nssv2393617, nssv2393620, nssv2393615, nssv2393616, nssv2393623, nssv2393618, nssv2393622, nssv2393619
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)nsv981104
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