A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859679



Internal ID22634614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66641966..66644313hg38UCSC Ensembl
chr8:67554201..67556548hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg382348
hg192348
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509703
Samples
Known GenesVCPIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859679
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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