A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006403



Internal ID20573443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107319447..107320013hg38UCSC Ensembl
chr13:107971795..107972361hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494386
Supporting Variants
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006403
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00053


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