A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433421



Internal ID21395423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35249174..35250146hg38UCSC Ensembl
chr22:35645167..35646139hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38973
hg19973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv485n172
Supporting Variantsnssv15752409, nssv15748289, nssv15751526, nssv15753147, nssv15753036, nssv15751893, nssv15750484, nssv15753639, nssv15747779, nssv15754665, nssv15754030, nssv15752348
SamplesNB12, SMI034, NB08, BTQ038, NB10, BTQ055, MDQ010, BTQ016, SMI041, NB07, SMI018, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433421
Frequency
Sample Size15
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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