A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746187



Internal ID20522198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108889233..108890387hg38UCSC Ensembl
chr6:109210436..109211590hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264382
Samples
Known GenesARMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746187
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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