A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866599



Internal ID22641534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101892039..101895296hg38UCSC Ensembl
chr8:102904267..102907524hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg383258
hg193258
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509466
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866599
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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