A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213580



Internal ID20780620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39423604..39530381hg38UCSC Ensembl
chr4:39425224..39532001hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38106778
hg19106778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391382
Supporting Variants
Samples
Known GenesKLB, LIAS, LOC401127, MIR1273H, RPL9, UGDH, UGDH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213580
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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