A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586736



Internal ID21535292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91328265..91330081hg38UCSC Ensembl
chr12:91722042..91723858hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086211
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586736
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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