A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417542



Internal ID22475412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157701927..157704281hg38UCSC Ensembl
chr3:157419716..157422070hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg382355
hg192355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905833
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417542
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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