A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741122



Internal ID20517099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124261355..124261476hg38UCSC Ensembl
chr12:124745901..124746022hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288364
Samples
Known GenesZNF664-FAM101A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741122
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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