A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023657



Internal ID20590697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41196256..41213256hg38UCSC Ensembl
chr15:41488454..41505454hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3817001
hg1917001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502957
Supporting Variants
Samples
Known GenesEXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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