A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854006



Internal ID22628941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98214333..98218851hg38UCSC Ensembl
chr8:99226561..99231079hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg384519
hg194519
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510312
Samples
Known GenesNIPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854006
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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