A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456267



Internal ID22514144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61816293..61817335hg38UCSC Ensembl
chr11:61583765..61584807hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381043
hg191043
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851041
Supporting Variants
Samples
Known GenesFADS1, FADS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456267
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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