A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024541



Internal ID20591581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44305279..44314344hg38UCSC Ensembl
chr15:44597477..44606542hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg389066
hg199066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497208
Supporting Variants
Samples
Known GenesCASC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024541
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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