A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367386



Internal ID22593055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32846829..32850900hg38UCSC Ensembl
chr11:32868375..32872446hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384072
hg194072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923750
Supporting Variants
Samples
Known GenesPRRG4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367386
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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