A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202384



Internal ID20769424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234098116..234098765hg38UCSC Ensembl
chr1:234233862..234234511hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321525
Supporting Variants
Samples
Known GenesSLC35F3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202384
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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