A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013168



Internal ID20580208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76793553..76800169hg38UCSC Ensembl
chr13:77367688..77374304hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg386617
hg196617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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