A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074122



Internal ID21489880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22339130..22339182hg38UCSC Ensembl
chr11:22360676..22360728hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591241
Supporting Variants
SamplesNA19238
Known GenesSLC17A6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074122
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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