A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075539



Internal ID21470421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59298763..59298819hg38UCSC Ensembl
chr11:59066236..59066292hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589873
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075539
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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