A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292903



Internal ID20502121
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 StatusS
Merged Variantsnsv4733492
Supporting Variants
Samples
Known GenesGPR85, LINC00998
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292903
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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