A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426346



Internal ID21083899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61984711..61987782hg38UCSC Ensembl
chr8:62897270..62900341hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg383072
hg193072
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426346
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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