A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024720



Internal ID20591760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48197401..48198800hg38UCSC Ensembl
chr15:48489598..48490997hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505870
Supporting Variants
Samples
Known GenesCTXN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024720
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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