A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110576



Internal ID20677616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:129140201..129147300hg38UCSC Ensembl
chr4:130061356..130068455hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391527
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00185


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