A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970095



Internal ID18605319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28731659..28732757hg38UCSC Ensembl
Innerchr6:28699436..28700534hg19UCSC Ensembl
Innerchr6:28807415..28808513hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2400645, nssv2400649, nssv2400642, nssv2400643, nssv2400646, nssv2400650, nssv2400651, nssv2400644, nssv2400648, nssv2400647
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)nsv970095
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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