A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970194



Internal ID18605418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168286849..168288791hg38UCSC Ensembl
Innerchr6:168687529..168689471hg19UCSC Ensembl
Innerchr6:168430378..168432320hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381943
hg191943
hg181943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2432327, nssv2432319, nssv2432318, nssv2432320, nssv2432324, nssv2432322, nssv2432325, nssv2432321, nssv2432326, nssv2432323
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)nsv970194
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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