A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487196



Internal ID21144749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67781908..67787663hg38UCSC Ensembl
chr13:68356040..68361795hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg385756
hg195756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18011858
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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