A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590330



Internal ID21538899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69853680..69853795hg38UCSC Ensembl
chr12:70247460..70247575hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081623
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590330
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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