A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293697



Internal ID20502915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10291330..10291437hg38UCSC Ensembl
chr2:10431456..10431563hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745894
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293697
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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