A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379839



Internal ID21037392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138230826..138231725hg38UCSC Ensembl
chr4:139151980..139152879hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213021
Samples
Known GenesSLC7A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379839
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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