A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490409



Internal ID21147962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68331578..68332216hg38UCSC Ensembl
chr13:68905710..68906348hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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