A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362095



Internal ID22587764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14829760..14830866hg38UCSC Ensembl
chr11:14851306..14852412hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381107
hg191107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926573
Supporting Variants
Samples
Known GenesPDE3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362095
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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