A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027926



Internal ID20594966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96924727..96925375hg38UCSC Ensembl
chr15:97467957..97468605hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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