A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897017



Internal ID22672114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32578935..32627376hg38UCSC Ensembl
chr3:32620427..32668868hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3848442
hg1948442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424516
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897017
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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