A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859118



Internal ID22634053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126235940..126239555hg38UCSC Ensembl
chr8:127248184..127251799hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg383616
hg193616
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506232, nssv17506233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859118
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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