A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033443



Internal ID21942786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122335426..122337228hg38UCSC Ensembl
chr12:122819973..122821775hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381803
hg191803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605258
Samples
Known GenesCLIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033443
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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