A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454098



Internal ID232202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23370912..23372274hg38UCSC Ensembl
chr7:23410531..23411893hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381363
hg191363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994182
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454098
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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