A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492776



Internal ID21150329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112039690..112049270hg38UCSC Ensembl
chr13:112694004..112703584hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg389581
hg199581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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