A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743952



Internal ID20519945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64280174..64280245hg38UCSC Ensembl
chr11:64047646..64047717hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272814
Samples
Known GenesBAD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743952
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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