A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027238



Internal ID20594278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84916882..84958875hg38UCSC Ensembl
chr15:85460113..85502106hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3841994
hg1941994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496919
Supporting Variants
Samples
Known GenesSLC28A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027238
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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