A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023736



Internal ID21933079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132780102..132780162hg38UCSC Ensembl
chr12:133356688..133356748hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603129
Samples
Known GenesGOLGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023736
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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