A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597378



Internal ID21789421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61908641..61908750hg38UCSC Ensembl
chr10:63668400..63668509hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014059
Supporting Variants
Samples
Known GenesARID5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597378
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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