A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479436



Internal ID256961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134683875..134689584hg38UCSC Ensembl
chr7:134368627..134374336hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg385710
hg195710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479436
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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