A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391810



Internal ID21049363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53971768..53994158hg38UCSC Ensembl
chr4:54837935..54860325hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3822391
hg1922391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117439
Samples
Known GenesRPL21P44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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