A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847694



Internal ID22622629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66166394..66171745hg38UCSC Ensembl
chr11:65933865..65939216hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385352
hg195352
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463381
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847694
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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