A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007865



Internal ID20574906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29702862..29703288hg38UCSC Ensembl
chr13:30276999..30277425hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00098


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