A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421561



Internal ID22479431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40712255..40712936hg38UCSC Ensembl
chr3:40753746..40754427hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421561
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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