A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383221



Internal ID21040774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42016422..42016669hg38UCSC Ensembl
chr5:42016524..42016771hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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