A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392582



Internal ID21050135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42819065..42823206hg38UCSC Ensembl
chr5:42819167..42823308hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg384142
hg194142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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