A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965745



Internal ID18600975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88274954..88278912hg38UCSC Ensembl
Innerchr6:88984673..88988631hg19UCSC Ensembl
Innerchr6:89041392..89045350hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383959
hg193959
hg183959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2417818, nssv2417819, nssv2417822, nssv2417814, nssv2417813, nssv2417817, nssv2417820, nssv2417821, nssv2417816, nssv2417815
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)nsv965745
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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