A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046591



Internal ID98872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61881699..61885727hg38UCSC Ensembl
chr11:61649171..61653199hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg384029
hg194029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497791
Supporting Variants
Samples
Known GenesFADS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046591
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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