A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926214



Internal ID22701441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29066090..29066698hg38UCSC Ensembl
chr8:28923607..28924215hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926214
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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