A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281520



Internal ID20490738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38936768..38936911hg38UCSC Ensembl
chr2:39163909..39164052hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746506
Supporting Variants
Samples
Known GenesARHGEF33
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281520
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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