A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287247



Internal ID20496465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92471922..92472242hg38UCSC Ensembl
chr4:93393073..93393393hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734954
Supporting Variants
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287247
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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