A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922055



Internal ID22697280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107368450..107368849hg38UCSC Ensembl
chr8:108380678..108381077hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444745
Samples
Known GenesANGPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922055
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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