A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17522156



Internal ID21846515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104099708..104114083hg38UCSC Ensembl
chr2:104716166..104730541hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3814376
hg1914376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5985280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17522156
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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