A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028726



Internal ID21938069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111811567..111811649hg38UCSC Ensembl
chr12:112249371..112249453hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028726
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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