A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981165



Internal ID18616364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89815010..89815624hg38UCSC Ensembl
Innerchr6:90524729..90525343hg19UCSC Ensembl
Innerchr6:90581450..90582064hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38615
hg19615
hg18615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2417331, nssv2417327, nssv2417326, nssv2417323, nssv2417329, nssv2417325, nssv2417324, nssv2417322, nssv2417330, nssv2417328
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMDN1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981165
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