A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482314



Internal ID21139867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77597135..77598053hg38UCSC Ensembl
chr13:78171270..78172188hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013219
Samples
Known GenesSCEL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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