A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965760



Internal ID18600990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:116455991..116459013hg38UCSC Ensembl
Innerchr6:116777154..116780176hg19UCSC Ensembl
Innerchr6:116883847..116886869hg18UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg383023
hg193023
hg183023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2421758, nssv2421755, nssv2421754, nssv2421762, nssv2421761, nssv2421757, nssv2421756, nssv2421759, nssv2421760, nssv2421753
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)nsv965760
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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