A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866973



Internal ID22641908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9931462..9934588hg38UCSC Ensembl
chr12:10084061..10087187hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg383127
hg193127
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457699
Samples
Known GenesCLEC2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866973
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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