A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292840



Internal ID20502058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113046490..113046544hg38UCSC Ensembl
chr3:112765337..112765391hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292840
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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