A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014309



Internal ID20581349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87108369..87153077hg38UCSC Ensembl
chr13:87760624..87805332hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3844709
hg1944709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494002
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014309
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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