A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919019



Internal ID22694241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26939516..27553947hg38UCSC Ensembl
chr8:26797033..27411464hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38614432
hg19614432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444352
Samples
Known GenesCHRNA2, EPHX2, MIR6842, PTK2B, STMN4, TRIM35
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919019
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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