A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490918



Internal ID21148471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97941287..97945384hg38UCSC Ensembl
chr13:98593541..98597638hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg384098
hg194098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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