A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390277



Internal ID22448147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63929523..63930847hg38UCSC Ensembl
chr20:62560876..62562200hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381325
hg191325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951824
Supporting Variants
Samples
Known GenesDNAJC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390277
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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