A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475915



Internal ID21133468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106381172..106386425hg38UCSC Ensembl
chr13:107033520..107038773hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385254
hg195254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475915
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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