A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047783



Internal ID99713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71412814..71412865hg38UCSC Ensembl
chr11:71123860..71123911hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394035
Supporting Variants
Samples
Known GenesFLJ42102
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047783
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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