A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271714



Internal ID20480932
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 StatusS
Merged Variantsnsv4747099
Supporting Variants
Samples
Known GenesUBE2T
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271714
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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