A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140900



Internal ID340094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137843381..137869381hg38UCSC Ensembl
chr4:138764535..138790535hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3826001
hg1926001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16955982
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140900
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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