A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493202



Internal ID21150755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60922763..60923439hg38UCSC Ensembl
chr13:61496897..61497573hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493202
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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