A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392376



Internal ID21049929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3437697..3443315hg38UCSC Ensembl
chr5:3437811..3443429hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg385619
hg195619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129721
Samples
Known GenesLINC01019
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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