A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746233



Internal ID20522244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100150642..100152780hg38UCSC Ensembl
chr3:99869486..99871624hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg382139
hg192139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295900
Samples
Known GenesCMSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746233
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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