A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459018



Internal ID237037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7433189..7509165hg38UCSC Ensembl
chr6:7433422..7509398hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3875977
hg1975977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459018
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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