A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394601



Internal ID21052154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5522371..5525694hg38UCSC Ensembl
chr5:5522484..5525807hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg383324
hg193324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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