A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178800



Internal ID20745840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57562120..58247494hg38UCSC Ensembl
chr13:58136254..58821628hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38685375
hg19685375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475900
Supporting Variants
Samples
Known GenesPCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178800
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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