A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877863



Internal ID22652828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:123239225..123627730hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38388506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv63n209
Supporting Variantsnssv17366075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877863
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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