A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059528



Internal ID20626568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240417012..240417688hg38UCSC Ensembl
chr1:240580312..240580988hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330862
Supporting Variants
Samples
Known GenesFMN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059528
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00667


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