A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750497



Internal ID20526453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3214852..3214852hg38UCSC Ensembl
chr11:3236082..3236082hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750497
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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