A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383505



Internal ID21041058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113965376..113965969hg38UCSC Ensembl
chr4:114886532..114887125hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106323
Samples
Known GenesARSJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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