A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848023



Internal ID22622958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94366729..94369371hg38UCSC Ensembl
chr8:95378957..95381599hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382643
hg192643
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848023
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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