A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008877



Internal ID20575919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39965260..39965643hg38UCSC Ensembl
chr13:40539397..40539780hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479711
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00101


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