A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025124



Internal ID21934467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105046148..105046205hg38UCSC Ensembl
chr12:105439926..105439983hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614494
Samples
Known GenesALDH1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025124
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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