A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390225



Internal ID21047778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105264201..105264800hg38UCSC Ensembl
chr4:106185358..106185957hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106966
Samples
Known GenesTET2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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