A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18011419



Internal ID20578459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67608452..67613520hg38UCSC Ensembl
chr13:68182584..68187652hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg385069
hg195069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493104
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18011419
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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