A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902684



Internal ID22677845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55518698..55518753hg38UCSC Ensembl
chr3:55552726..55552781hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414019
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902684
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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