A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936272



Internal ID22711624
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 StatusM
Merged Variants
Supporting Variantsnssv17364117
Samples
Known GenesARHGEF7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936272
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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