A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408275



Internal ID22466145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101690538..101692960hg38UCSC Ensembl
chr3:101409382..101411804hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg382423
hg192423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892395
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408275
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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