A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18012803



Internal ID20579843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72738265..72738838hg38UCSC Ensembl
chr13:73312403..73312976hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491544
Supporting Variants
Samples
Known GenesBORA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18012803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0004


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