A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748427



Internal ID20524452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64500960..64501020hg38UCSC Ensembl
chr11:64268432..64268492hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748427
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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