A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751255



Internal ID20527115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31061577..31061577hg38UCSC Ensembl
chr12:31214511..31214511hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262357
Samples
Known GenesDDX11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751255
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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