A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864338



Internal ID22639273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47426865..47484201hg38UCSC Ensembl
chr8:48339427..48396763hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3857337
hg1957337
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509255
Samples
Known GenesSPIDR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864338
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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