A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554904



Internal ID20927994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44867046..44868319hg38UCSC Ensembl
chr22:45262926..45264199hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381274
hg191274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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