A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863175



Internal ID22638110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94641721..94647075hg38UCSC Ensembl
chr11:94374887..94380241hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385355
hg195355
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464278
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863175
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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