A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024693



Internal ID21934036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101100535..101101579hg38UCSC Ensembl
chr12:101494313..101495357hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381045
hg191045
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600300
Samples
Known GenesANO4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024693
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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