A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705285



Internal ID21377561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12413024..12413197hg38UCSC Ensembl
chr12:12565958..12566131hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390134
Supporting Variants
Samples
Known GenesLOH12CR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705285
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0172414


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