A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755002



Internal ID20530862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103768495..103768495hg38UCSC Ensembl
chr12:104162273..104162273hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755002
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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