A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732032



Internal ID20507954
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 StatusM
Merged Variants
Supporting Variantsnssv16271201
Samples
Known GenesCPXM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732032
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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