A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141277



Internal ID340472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181353324..181364000hg38UCSC Ensembl
chr5:180780325..180791001hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3810677
hg1910677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv414n206
Supporting Variantsnssv16977912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141277
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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