A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733492



Internal ID20509422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112981186..113498722hg38UCSC Ensembl
chr7:112621241..113138777hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38517537
hg19517537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292903
Samples
Known GenesGPR85, LINC00998
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733492
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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