A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555687



Internal ID328838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60727812..60727846hg38UCSC Ensembl
chr11:60495285..60495319hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555687
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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