A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5399699



Internal ID179087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61179847..61179898hg38UCSC Ensembl
chr11:60947319..60947370hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5399699
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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