A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074912



Internal ID20641952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37543538..37586521hg38UCSC Ensembl
chr22:37939545..37982528hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3842984
hg1942984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541398
Supporting Variants
Samples
Known GenesCDC42EP1, LGALS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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