A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015589



Internal ID20582629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96202381..96206194hg38UCSC Ensembl
chr13:96854635..96858448hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg383814
hg193814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482507
Supporting Variants
Samples
Known GenesHS6ST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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