A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541612



Internal ID21865967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29576209..29579308hg38UCSC Ensembl
chr3:29617700..29620799hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993561
Supporting Variants
Samples
Known GenesRBMS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541612
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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