A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969400



Internal ID18604627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:50702673..50704527hg38UCSC Ensembl
Innerchr6:50670386..50672240hg19UCSC Ensembl
Innerchr6:50778345..50780199hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381855
hg191855
hg181855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2409796, nssv2409803, nssv2409797, nssv2409795, nssv2409802, nssv2409800, nssv2409804, nssv2409801, nssv2409799, nssv2409798
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)nsv969400
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