A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505096



Internal ID22563040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20273847..20279911hg38UCSC Ensembl
chr8:20131358..20137422hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg386065
hg196065
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852197
Supporting Variants
Samples
Known GenesLZTS1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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