A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425708



Internal ID21083261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92749835..92750432hg38UCSC Ensembl
chr8:93762063..93762660hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173480
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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