A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981189



Internal ID18616388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:136973186..136975150hg38UCSC Ensembl
Innerchr6:137294323..137296287hg19UCSC Ensembl
Innerchr6:137336016..137337980hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381965
hg191965
hg181965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2426107, nssv2426112, nssv2426105, nssv2426106, nssv2426110, nssv2426111, nssv2426109, nssv2426104, nssv2426108, nssv2426113
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)nsv981189
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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