A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351078



Internal ID22576747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93621563..93629279hg38UCSC Ensembl
chr11:93354729..93362445hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg387717
hg197717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351078
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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