A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418409



Internal ID21075962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92768022..92768612hg38UCSC Ensembl
chr8:93780250..93780840hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173482
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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