A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184452



Internal ID20751492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37152501..37156000hg38UCSC Ensembl
chr13:37726638..37730137hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184452
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0004


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