A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360218



Internal ID22585887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93286999..93296739hg38UCSC Ensembl
chr11:93020165..93029905hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389741
hg199741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360218
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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