A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931110



Internal ID21489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15046819..15047014hg38UCSC Ensembl
chr3:15088326..15088521hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443202
Supporting Variants
Samples
Known GenesNR2C2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931110
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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