A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921808



Internal ID22697032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36963792..36985521hg38UCSC Ensembl
chr8:36821310..36843039hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3821730
hg1921730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921808
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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