A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920213



Internal ID22695436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102331553..102332919hg38UCSC Ensembl
chr11:102202284..102203650hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381367
hg191367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364987
Samples
Known GenesBIRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920213
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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