A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18055210



Internal ID20622250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190219592..190219841hg38UCSC Ensembl
chr1:190188722..190188971hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332981
Supporting Variants
Samples
Known GenesBRINP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18055210
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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