A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389350



Internal ID21046903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107588501..107593900hg38UCSC Ensembl
chr4:108509658..108515056hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg385400
hg195399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5404n223
Supporting Variantsnssv18105804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389350
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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