A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739290



Internal ID20515263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8201279..8201335hg38UCSC Ensembl
chr11:8222826..8222882hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739290
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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