A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888016



Internal ID22663016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9994085..10047814hg38UCSC Ensembl
chr3:10035769..10089498hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3853730
hg1953730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415490
Samples
Known GenesCIDECP, EMC3-AS1, FANCD2, LOC401052
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888016
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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