A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721038



Internal ID144704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7396581..7398477hg38UCSC Ensembl
chr19:7461467..7463363hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381897
hg191897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521042
Supporting Variants
Samples
Known GenesARHGEF18
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721038
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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