A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923933



Internal ID22699160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22964533..22976211hg38UCSC Ensembl
chr7:23004152..23015830hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3811679
hg1911679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442288
Samples
Known GenesFAM126A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923933
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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