A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380825



Internal ID21038378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119487401..119489800hg38UCSC Ensembl
chr4:120408556..120410955hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107201
Samples
Known GenesLOC645513
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380825
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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