A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394022



Internal ID21051575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77562591..77562710hg38UCSC Ensembl
chr4:78483745..78483864hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120311
Samples
Known GenesCXCL13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394022
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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