A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008402



Internal ID20575442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37139416..37139921hg38UCSC Ensembl
chr13:37713553..37714058hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00105


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