A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742799



Internal ID20518784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46326826..46327146hg38UCSC Ensembl
chr7:46366424..46366744hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742799
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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