A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490859



Internal ID21148412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59200485..59201214hg38UCSC Ensembl
chr13:59774619..59775348hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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