A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489852



Internal ID21147405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108307768..108310865hg38UCSC Ensembl
chr13:108960116..108963213hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg383098
hg193098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006487
Samples
Known GenesTNFSF13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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