A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602495



Internal ID21551153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18350483..18350589hg38UCSC Ensembl
chr11:18372030..18372136hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073847
SamplesHG01114
Known GenesGTF2H1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602495
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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