A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379242



Internal ID21036795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31367261..31367394hg38UCSC Ensembl
chr5:31367368..31367501hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130881
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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