A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402648



Internal ID21060201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111151851..111158116hg38UCSC Ensembl
chr5:110487549..110493814hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg386266
hg196266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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