A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484266



Internal ID261683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85402115..85502608hg38UCSC Ensembl
chr7:85031431..85131924hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38100494
hg19100494
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484266
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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