A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189283



Internal ID20756323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107865701..107868700hg38UCSC Ensembl
chr13:108518049..108521048hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494906
Supporting Variants
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189283
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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