A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284093



Internal ID20493311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17853277..17853354hg38UCSC Ensembl
chr2:18034544..18034621hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284093
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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