A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012501



Internal ID21921844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83357214..83357279hg38UCSC Ensembl
chr9:85972129..85972194hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594262
Samples
Known GenesFRMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012501
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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