A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854338



Internal ID22629273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11534635..11554010hg38UCSC Ensembl
chr8:11392144..11411519hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3819376
hg1919376
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1987n209
Supporting Variantsnssv17505576
Samples
Known GenesBLK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854338
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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