A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008545



Internal ID20575586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46785301..46787300hg38UCSC Ensembl
chr13:47359436..47361435hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492981
Supporting Variants
Samples
Known GenesESD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008545
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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