A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202327



Internal ID20769367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198892886..198991243hg38UCSC Ensembl
chr1:198862015..198960372hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3898358
hg1998358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324016
Supporting Variants
Samples
Known GenesMIR181A1HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202327
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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