A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423395



Internal ID22481265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48168284..48169758hg38UCSC Ensembl
chr3:48209774..48211248hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381475
hg191475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887983
Supporting Variants
Samples
Known GenesCDC25A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423395
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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