A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585156



Internal ID21533701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110058466..110058637hg38UCSC Ensembl
chr12:110496271..110496442hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17077130
SamplesHG03486
Known GenesC12orf76
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585156
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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