A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494769



Internal ID21152322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68519260..68605790hg38UCSC Ensembl
chr13:69093392..69179922hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3886531
hg1986531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494769
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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