A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140951



Internal ID340145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:111894700..111901381hg38UCSC Ensembl
chr4:112815856..112822537hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg386682
hg196682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv378n206
Supporting Variantsnssv16955027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140951
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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