A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488705



Internal ID21146258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105134855..105150952hg38UCSC Ensembl
chr13:105787206..105803303hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3816098
hg1916098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006873
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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