A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585300



Internal ID21533846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17022322..17027362hg38UCSC Ensembl
chr12:17175256..17180296hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg385041
hg195041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17078811
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585300
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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