A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965689



Internal ID18254233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26456805..26469259hg38UCSC Ensembl
Innerchr6:26457033..26469487hg19UCSC Ensembl
Innerchr6:26565012..26577466hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3812455
hg1912455
hg1812455
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2397882, nssv2397878, nssv2397881, nssv2397880, nssv2397876, nssv2397875, nssv2397879, nssv2397874, nssv2397877, nssv2397873
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesBTN2A1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965689
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