A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586746



Internal ID21535302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:33111485..33113422hg38UCSC Ensembl
chr12:33264419..33266356hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg381938
hg191938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098262
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586746
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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