A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029806



Internal ID87580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138255468..138334600hg38UCSC Ensembl
chr11:72884..149569hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3879133
hg1976686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142084
Supporting Variants
Samples
Known GenesLINC01001
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029806
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000876


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