A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478871



Internal ID21136424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107035553..107038185hg38UCSC Ensembl
chr13:107687901..107690533hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg382633
hg192633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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