A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549605



Internal ID21873960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32115262..32115324hg38UCSC Ensembl
chr3:32156754..32156816hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993095
Supporting Variants
Samples
Known GenesGPD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549605
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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