A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730037



Internal ID153703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157337544..157338601hg38UCSC Ensembl
chr2:158194056..158195113hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg381058
hg191058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452681
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730037
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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