A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743789



Internal ID20519779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34537294..34537356hg38UCSC Ensembl
chr11:34558841..34558903hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743789
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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