A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459581



Internal ID22517466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49199094..49211994hg38UCSC Ensembl
chr11:49220646..49233546hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3812901
hg1912901
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855311
Supporting Variants
Samples
Known GenesFOLH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459581
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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