A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388099



Internal ID22445969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79761595..79765958hg38UCSC Ensembl
chr13:80335730..80340093hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg384364
hg194364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5946922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388099
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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