A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034289



Internal ID21943632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22575430..22581418hg38UCSC Ensembl
chr12:22728364..22734352hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg385989
hg195989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034289
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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