A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073706



Internal ID20640746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30922060..30922916hg38UCSC Ensembl
chr22:31318047..31318903hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540131
Supporting Variants
Samples
Known GenesMORC2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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