A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038607



Internal ID21947950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109902752..109912079hg38UCSC Ensembl
chr12:110340557..110349884hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg389328
hg199328
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616986
Samples
Known GenesTCHP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038607
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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