A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433710



Internal ID21395712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238591710..238593091hg38UCSC Ensembl
chr2:239500351..239501732hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381382
hg191382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv443n172
Supporting Variantsnssv15752691, nssv15745943
SamplesBTQ016, SMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433710
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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