A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549852



Internal ID21874207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185210390..185210442hg38UCSC Ensembl
chr4:186131544..186131596hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996275
Supporting Variants
Samples
Known GenesSNX25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549852
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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