A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601502



Internal ID21550149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73896833..73897011hg38UCSC Ensembl
chr11:73607878..73608056hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076044
SamplesNA19238
Known GenesPAAF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601502
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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