A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268137



Internal ID20477355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101468992..101469043hg38UCSC Ensembl
chr2:102085454..102085505hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733924
Supporting Variants
Samples
Known GenesRFX8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268137
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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