A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930156



Internal ID20847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14492604..14493389hg38UCSC Ensembl
chr3:14534112..14534897hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451449
Supporting Variants
Samples
Known GenesGRIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930156
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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