A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990475



Internal ID20557516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37472501..37473600hg38UCSC Ensembl
chr11:37494051..37495150hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990475
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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