A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007229



Internal ID20574269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107791692..107792286hg38UCSC Ensembl
chr13:108444040..108444634hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493053
Supporting Variants
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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