A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287921



Internal ID20497139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124826954..124827012hg38UCSC Ensembl
chr10:126515523..126515581hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740424
Supporting Variants
Samples
Known GenesFAM175B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287921
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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