A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392401



Internal ID21049954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106254501..106257100hg38UCSC Ensembl
chr4:107175658..107178257hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209487
Samples
Known GenesTBCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392401
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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