A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025168



Internal ID20592208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50280314..50283258hg38UCSC Ensembl
chr15:50572511..50575455hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg382945
hg192945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502882
Supporting Variants
Samples
Known GenesGABPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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