A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072195



Internal ID21505928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118607365..118609844hg38UCSC Ensembl
chr11:118478080..118480559hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382480
hg192480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595537
Supporting Variants
SamplesNA19983
Known GenesPHLDB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072195
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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