A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597807



Internal ID21546426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39093920..39094244hg38UCSC Ensembl
chr11:39115470..39115794hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074924
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597807
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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