A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969455



Internal ID18604682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149399709..149406119hg38UCSC Ensembl
Innerchr6:149720845..149727255hg19UCSC Ensembl
Innerchr6:149762538..149768948hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg386411
hg196411
hg186411
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2426583, nssv2426575, nssv2426581, nssv2426577, nssv2426574, nssv2426582, nssv2426576, nssv2426578, nssv2426580, nssv2426579
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSUMO4, TAB2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969455
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