A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543345



Internal ID21867700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151685750..151701583hg38UCSC Ensembl
chr3:151403538..151419371hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3815834
hg1915834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991669
Supporting Variants
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543345
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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