A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388123



Internal ID21045676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150392444..150395750hg38UCSC Ensembl
chr4:151313596..151316902hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383307
hg193307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112841
Samples
Known GenesLRBA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388123
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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