A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449741



Internal ID22507611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34131290..34132326hg38UCSC Ensembl
chr11:34152837..34153873hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381037
hg191037
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858610
Supporting Variants
Samples
Known GenesNAT10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449741
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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