A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364117



Internal ID22589786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111221214..111221419hg38UCSC Ensembl
chr13:111873561..111873766hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936272
Supporting Variants
Samples
Known GenesARHGEF7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364117
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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