A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384551



Internal ID21042104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75941630..75944718hg38UCSC Ensembl
chr4:76862783..76865871hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg383089
hg193089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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