A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036880



Internal ID21946223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54201879..54203004hg38UCSC Ensembl
chr12:54595663..54596788hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036880
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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