A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746839



Internal ID20522854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108859847..108859930hg38UCSC Ensembl
chr12:109253623..109253706hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746839
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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