A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487308



Internal ID22545224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62166720..62171669hg38UCSC Ensembl
chr20:60741776..60746725hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384950
hg194950
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868279
Supporting Variants
Samples
Known GenesSS18L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487308
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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