A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024111



Internal ID20591151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38523834..38524400hg38UCSC Ensembl
chr15:38816035..38816601hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513686
Supporting Variants
Samples
Known GenesRASGRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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