A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025169



Internal ID20592209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50281457..50285683hg38UCSC Ensembl
chr15:50573654..50577880hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg384227
hg194227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505188
Supporting Variants
Samples
Known GenesGABPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025169
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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