A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008384



Internal ID20575424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36718871..36727288hg38UCSC Ensembl
chr13:37293008..37301425hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg388418
hg198418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494940
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008384
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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