A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016844



Internal ID21926187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23427984..23443732hg38UCSC Ensembl
chr7:23467603..23483351hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3815749
hg1915749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564431
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016844
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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