A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587245



Internal ID21535805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9953407..9953472hg38UCSC Ensembl
chr12:10106006..10106071hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094407
SamplesNA18939
Known GenesCLEC12A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587245
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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