A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140609



Internal ID339802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177829324..177855324hg38UCSC Ensembl
chr5:177256325..177282325hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3826001
hg1926001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140609
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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