A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537569



Internal ID21861924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53194981..53196101hg38UCSC Ensembl
chr4:54061148..54062268hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997607
Supporting Variants
Samples
Known GenesSCFD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537569
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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