A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214417



Internal ID20781457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99562564..99562860hg38UCSC Ensembl
chr4:100483721..100484017hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391916
Supporting Variants
Samples
Known GenesTRMT10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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