A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390134



Internal ID21381269
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 StatusM
Merged Variants
Supporting Variantsnssv15705285
Samples
Known GenesLOH12CR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390134
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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