A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046527



Internal ID98830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61122658..61122705hg38UCSC Ensembl
chr11:60890130..60890177hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554522
Supporting Variants
Samples
Known GenesCD5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046527
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer