A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383920



Internal ID21041473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:30337523..30350110hg38UCSC Ensembl
chr5:30337630..30350217hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3812588
hg1912588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383920
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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