A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376124



Internal ID21033677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3460779..3463291hg38UCSC Ensembl
chr5:3460893..3463405hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382513
hg192513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129734
Samples
Known GenesLINC01019
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376124
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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