A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418396



Internal ID21075949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61363876..61373462hg38UCSC Ensembl
chr8:62276435..62286021hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg389587
hg199587
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235401
Samples
Known GenesCLVS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418396
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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