A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213025



Internal ID20780065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138928001..138933200hg38UCSC Ensembl
chr4:139849155..139854354hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213025
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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