A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546005



Internal ID21870360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181975577..181975729hg38UCSC Ensembl
chr4:182896730..182896882hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996780
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546005
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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