A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022628



Internal ID21931971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108436081..108439875hg38UCSC Ensembl
chr12:108829858..108833652hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg383795
hg193795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022628
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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