A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940063



Internal ID27427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157065461..157067144hg38UCSC Ensembl
chr3:156783250..156784933hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940063
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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