A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007655



Internal ID20574695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20223037..20531805hg38UCSC Ensembl
chr13:20797176..21105944hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38308769
hg19308769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488809
Supporting Variants
Samples
Known GenesCRYL1, GJB6, MIR4499
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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