A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863929



Internal ID22638864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104284975..104292913hg38UCSC Ensembl
chr8:105297203..105305141hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg387939
hg197939
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504858
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863929
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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