A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380231



Internal ID21037784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74989378..74991891hg38UCSC Ensembl
chr4:75914588..75917101hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382514
hg192514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5338n223
Supporting Variantsnssv18121020
Samples
Known GenesPARM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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