A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190567



Internal ID20757607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28904940..28909428hg38UCSC Ensembl
chr13:29479077..29483565hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg384489
hg194489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490157
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190567
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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