A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969374



Internal ID18257915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:30025056..30033766hg38UCSC Ensembl
Innerchr6:29992833..30001543hg19UCSC Ensembl
Innerchr6:30100812..30109522hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg388711
hg198711
hg188711
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2404033, nssv2404035, nssv2404037, nssv2404032, nssv2404034, nssv2404038, nssv2404039, nssv2404031, nssv2404036, nssv2404040
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesZNRD1-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969374
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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