A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409934



Internal ID22467804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194243793..194245062hg38UCSC Ensembl
chr3:193961582..193962851hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381270
hg191270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409934
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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