A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474111



Internal ID251779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108605139..108605378hg38UCSC Ensembl
chr7:108245583..108245822hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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