A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135137



Internal ID20702177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77696070..77696643hg38UCSC Ensembl
chr5:76991895..76992468hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412188
Supporting Variants
Samples
Known GenesTBCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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