A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574326



Internal ID21522741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81014531..81014973hg38UCSC Ensembl
chr3:81063682..81064124hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133407
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574326
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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