A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848619



Internal ID22623554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101836304..101859100hg38UCSC Ensembl
chr8:102848532..102871328hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3822797
hg1922797
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504306
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848619
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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