A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436583



Internal ID22494453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20273908..20280002hg38UCSC Ensembl
chr8:20131419..20137513hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg386095
hg196095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921791
Supporting Variants
Samples
Known GenesLZTS1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436583
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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