A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360248



Internal ID22585917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3217508..3222855hg38UCSC Ensembl
chr11:3238738..3244085hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385348
hg195348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910635
Supporting Variants
Samples
Known GenesMRGPRG, MRGPRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360248
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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