A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866826



Internal ID22641761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124734901..124736500hg38UCSC Ensembl
chr8:125747143..125748742hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2029n209
Supporting Variantsnssv17506207, nssv17506206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866826
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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