A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184836



Internal ID20751876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57699501..57707400hg38UCSC Ensembl
chr13:58273635..58281534hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488189
Supporting Variants
Samples
Known GenesPCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184836
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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