A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260681



Internal ID20469899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32122256..32122307hg38UCSC Ensembl
chr20:30710059..30710110hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736678
Supporting Variants
Samples
Known GenesTM9SF4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260681
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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