A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970087



Internal ID18258625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26392104..26397135hg38UCSC Ensembl
Innerchr6:26392332..26397363hg19UCSC Ensembl
Innerchr6:26500311..26505342hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg385032
hg195032
hg185032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2398171, nssv2398175, nssv2398172, nssv2398178, nssv2398170, nssv2398174, nssv2398179, nssv2398177, nssv2398176, nssv2398173
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesBTN2A2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970087
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