A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18055262



Internal ID20622302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193280240..193284083hg38UCSC Ensembl
chr1:193249370..193253213hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg383844
hg193844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18055262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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