A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488637



Internal ID21146190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79459470..79465103hg38UCSC Ensembl
chr13:80033605..80039238hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg385634
hg195634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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