A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461317



Internal ID22519200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97564469..97614266hg38UCSC Ensembl
chr11:97435469..97485266hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3849798
hg1949798
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855269
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461317
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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