A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940538



Internal ID27744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150605459..150605548hg38UCSC Ensembl
chr3:150323246..150323335hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442917
Supporting Variants
Samples
Known GenesSELT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940538
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001873


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