A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026019



Internal ID21935362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25668614..25668666hg38UCSC Ensembl
chr12:25821548..25821600hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026019
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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