A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565303



Internal ID21513615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38113449..38113583hg38UCSC Ensembl
chr3:38154940..38155074hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128848
SamplesHG00171
Known GenesDLEC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565303
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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