A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861610



Internal ID22636545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109906163..109908712hg38UCSC Ensembl
chr11:109776889..109779438hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861610
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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