A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747099



Internal ID20523116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202338378..202338444hg38UCSC Ensembl
chr1:202307506..202307572hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271714
Samples
Known GenesUBE2T
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747099
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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