A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369552



Internal ID21027105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20435412..20443868hg38UCSC Ensembl
chr4:20437035..20445491hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg388457
hg198457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113242
Samples
Known GenesSLIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369552
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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