A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547136



Internal ID21871491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:118718300..118718729hg38UCSC Ensembl
chr3:118437147..118437576hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991466
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547136
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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