A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462487



Internal ID22520372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63931430..63934088hg38UCSC Ensembl
chr11:63698902..63701560hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382659
hg192659
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853233
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462487
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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