A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191700



Internal ID20758740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108080401..108081700hg38UCSC Ensembl
chr13:108732749..108734048hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480714
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191700
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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