A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918087



Internal ID22693308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130418177..130418279hg38UCSC Ensembl
chr11:130288072..130288174hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366296
Samples
Known GenesADAMTS8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918087
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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