A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17522604



Internal ID21846963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:232897803..232897923hg38UCSC Ensembl
chr2:233762513..233762633hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987958
Supporting Variants
Samples
Known GenesNGEF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17522604
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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