A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913885



Internal ID22689101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66166427..66171858hg38UCSC Ensembl
chr11:65933898..65939329hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385432
hg195432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356584
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913885
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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