A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026302



Internal ID21935645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27009179..27009446hg38UCSC Ensembl
chr12:27162112..27162379hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608494
Samples
Known GenesTM7SF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026302
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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