A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922874



Internal ID22698099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107389239..107389332hg38UCSC Ensembl
chr7:107029684..107029777hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434415
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922874
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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