A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580321



Internal ID21772364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124050476..124050706hg38UCSC Ensembl
chr8:125062717..125062947hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006920
Supporting Variants
Samples
Known GenesFER1L6, FER1L6-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580321
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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