A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029000



Internal ID21938343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122124322..122124408hg38UCSC Ensembl
chr12:122608869..122608955hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616062
Samples
Known GenesMLXIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029000
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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