A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864322



Internal ID22639257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102526156..102538839hg38UCSC Ensembl
chr8:103538384..103551067hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3812684
hg1912684
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864322
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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