A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073751



Internal ID20640791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31821611..31823464hg38UCSC Ensembl
chr22:32217597..32219450hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381854
hg191854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549368
Supporting Variants
Samples
Known GenesDEPDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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