A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542955



Internal ID21867310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86416942..86418094hg38UCSC Ensembl
chr3:86466092..86467244hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994254
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542955
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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