A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744975



Internal ID20520979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60604634..60604855hg38UCSC Ensembl
chr11:60372107..60372328hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294847
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744975
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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