A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032429



Internal ID21941772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93375470..93375529hg38UCSC Ensembl
chr12:93769246..93769305hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605673
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032429
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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