A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477046



Internal ID21134599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106820625..106821327hg38UCSC Ensembl
chr13:107472973..107473675hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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