A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859244



Internal ID22634179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70102190..70106302hg38UCSC Ensembl
chr8:71014425..71018537hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg384113
hg194113
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859244
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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