A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007202



Internal ID20574242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107573958..107574538hg38UCSC Ensembl
chr13:108226306..108226886hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494842
Supporting Variants
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007202
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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