A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140687



Internal ID339880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181403700..181477493hg38UCSC Ensembl
chr5:180830701..180904494hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3873794
hg1973794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv415n206
Supporting Variantsnssv16977913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140687
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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