A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013157



Internal ID20580197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76666488..76666903hg38UCSC Ensembl
chr13:77240623..77241038hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485260
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00053


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