A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189165



Internal ID20756205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28538075..28539443hg38UCSC Ensembl
chr13:29112212..29113580hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg381369
hg191369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495546
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189165
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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