A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554159



Internal ID20927266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48298850..48304220hg38UCSC Ensembl
chr22:48694662..48700032hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg385371
hg195371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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