A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015434



Internal ID20582474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96276987..96406030hg38UCSC Ensembl
chr13:96929241..97058284hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38129044
hg19129044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491530
Supporting Variants
Samples
Known GenesHS6ST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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