A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008551



Internal ID20575592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46859469..46860263hg38UCSC Ensembl
chr13:47433604..47434398hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492307
Supporting Variants
Samples
Known GenesHTR2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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