A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023659



Internal ID20590699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41213960..41214767hg38UCSC Ensembl
chr15:41506158..41506965hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514177
Supporting Variants
Samples
Known GenesEXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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