A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486656



Internal ID22544571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53153240..53166165hg38UCSC Ensembl
chr20:51769779..51782704hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3812926
hg1912926
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872648
Supporting Variants
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486656
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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