A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862473



Internal ID22637408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103313124..103314566hg38UCSC Ensembl
chr8:104325352..104326794hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381443
hg191443
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504851
Samples
Known GenesFZD6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862473
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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