A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862467



Internal ID22637402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95086945..95090674hg38UCSC Ensembl
chr8:96099173..96102902hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383730
hg193730
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510275
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862467
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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