A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388856



Internal ID21046409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18305188..18330852hg38UCSC Ensembl
chr5:18305297..18330961hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3825665
hg1925665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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