A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753621



Internal ID20529481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77778112..77778112hg38UCSC Ensembl
chr11:77489158..77489158hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263537
Samples
Known GenesRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753621
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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