A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054898



Internal ID20621938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190472866..190473545hg38UCSC Ensembl
chr1:190441996..190442675hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335040
Supporting Variants
Samples
Known GenesBRINP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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