A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970084



Internal ID18605308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26183711..26184355hg38UCSC Ensembl
Innerchr6:26183939..26184583hg19UCSC Ensembl
Innerchr6:26291918..26292562hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38645
hg19645
hg18645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2396365, nssv2396360, nssv2396361, nssv2396362, nssv2396366, nssv2396367, nssv2396368, nssv2396364, nssv2396363, nssv2396359
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHIST1H2BE
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970084
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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