A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059955



Internal ID20626995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28523320..28525445hg38UCSC Ensembl
chr1:28849832..28851957hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382126
hg192126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325525
Supporting Variants
Samples
Known GenesRCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00065


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