A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763773



Internal ID20539633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44296934..44296934hg38UCSC Ensembl
chr6:44264671..44264671hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272288
Samples
Known GenesTCTE1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763773
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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