A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281714



Internal ID20490932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190690001..190690001hg38UCSC Ensembl
chr2:191554727..191554727hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751156
Supporting Variants
Samples
Known GenesNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281714
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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