A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17539177



Internal ID21863532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176652835..176652919hg38UCSC Ensembl
chr4:177573986..177574070hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17539177
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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