A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008878



Internal ID20575920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39973250..39973881hg38UCSC Ensembl
chr13:40547387..40548018hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38632
hg19632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491575
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008878
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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