A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848971



Internal ID22623906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104462465..104464096hg38UCSC Ensembl
chr8:105474693..105476324hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381632
hg191632
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509491
Samples
Known GenesDPYS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848971
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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