A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735545



Internal ID20511488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62653778..62653845hg38UCSC Ensembl
chr11:62421250..62421317hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735545
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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