A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027219



Internal ID21936562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122357743..122357873hg38UCSC Ensembl
chr12:122842290..122842420hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616773
Samples
Known GenesCLIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027219
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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