A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855372



Internal ID22630307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43123720..43127469hg38UCSC Ensembl
chr8:42978863..42982612hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg383750
hg193750
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855372
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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