A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890686



Internal ID22665714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127373559..127373706hg38UCSC Ensembl
chr3:127092402..127092549hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890686
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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