A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482691



Internal ID21140244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:64802365..64914517hg38UCSC Ensembl
chr13:65376497..65488649hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38112153
hg19112153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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