A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923213



Internal ID22698439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66618507..66624256hg38UCSC Ensembl
chr8:67530742..67536491hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg385750
hg195750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923213
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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