A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072861



Internal ID21484384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117548667..117549853hg38UCSC Ensembl
chr11:117419382..117420568hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381187
hg191187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603859
Supporting Variants
SamplesNA12329
Known GenesDSCAML1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072861
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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