A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493560



Internal ID21151113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31110072..31126189hg38UCSC Ensembl
chr13:31684209..31700326hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3816118
hg1916118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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