A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059583



Internal ID20626623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24366115..24366461hg38UCSC Ensembl
chr1:24692605..24692951hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322672
Supporting Variants
Samples
Known GenesSTPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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