A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141127



Internal ID340322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:111893381..111901381hg38UCSC Ensembl
chr4:112814537..112822537hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv378n206
Supporting Variantsnssv17735151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141127
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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