A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909762



Internal ID22684972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22161452..22161501hg38UCSC Ensembl
chr7:22201070..22201119hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432754
Samples
Known GenesRAPGEF5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909762
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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