A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908589



Internal ID22683799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106534618..106535016hg38UCSC Ensembl
chr7:106175064..106175462hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908589
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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