A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045566



Internal ID98140
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 StatusS
Merged Variantsnsv5555687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045566
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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