A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287282



Internal ID20496500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61908605..61908704hg38UCSC Ensembl
chr10:63668364..63668463hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732043
Supporting Variants
Samples
Known GenesARID5B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287282
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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