A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290806



Internal ID20500024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57482451..57482531hg38UCSC Ensembl
chr2:57709586..57709666hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290806
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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