A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867287



Internal ID22642222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30994039..30996038hg38UCSC Ensembl
chr8:30851555..30853554hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509125
Samples
Known GenesPURG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867287
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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