A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433693



Internal ID21395695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22235179..22241949hg38UCSC Ensembl
chr2:22458051..22464821hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg386771
hg196771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752838
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433693
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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