A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392402



Internal ID21049955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8268240..8292255hg38UCSC Ensembl
chr5:8268353..8292368hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3824016
hg1924016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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