A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008706



Internal ID20575747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39558507..39566622hg38UCSC Ensembl
chr13:40132644..40140759hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg388116
hg198116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484252
Supporting Variants
Samples
Known GenesLHFP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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