A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757868



Internal ID20533728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45738304..45738304hg38UCSC Ensembl
chr11:45759855..45759855hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757868
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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