A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072938



Internal ID21489202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125139098..125139168hg38UCSC Ensembl
chr11:125008994..125009064hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592347
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072938
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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