A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271201



Internal ID20480419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123857544..123857649hg38UCSC Ensembl
chr10:125617060..125617165hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732032
Supporting Variants
Samples
Known GenesCPXM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271201
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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