A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745272



Internal ID20521279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39217024..39217088hg38UCSC Ensembl
chr21:40588950..40589014hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262170
Samples
Known GenesBRWD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745272
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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