A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923215



Internal ID22698441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98686820..98686891hg38UCSC Ensembl
chr7:98316132..98316203hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923215
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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