A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075394



Internal ID21498273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57986972..57994634hg38UCSC Ensembl
chr11:57754444..57762106hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg387663
hg197663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593294
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075394
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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