A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764733



Internal ID20540593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134190900..134190900hg38UCSC Ensembl
chr7:133875652..133875652hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289928
Samples
Known GenesLRGUK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764733
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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