A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940071



Internal ID27431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157156712..157175484hg38UCSC Ensembl
chr3:156874501..156893273hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3818773
hg1918773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441859
Supporting Variants
Samples
Known GenesCCNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940071
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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