A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380874



Internal ID21038427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97239542..97282201hg38UCSC Ensembl
chr4:98160693..98203352hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3842660
hg1942660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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