A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461522



Internal ID22519407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98686040..98687039hg38UCSC Ensembl
chr11:98556770..98557769hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863669
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461522
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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