A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075563



Internal ID21461540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60201224..60201273hg38UCSC Ensembl
chr11:59968697..59968746hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587112
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075563
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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