A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918218



Internal ID22693439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:60340802..62512424hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382171623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1876n209
Supporting Variantsnssv17434667
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918218
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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