A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847827



Internal ID22622762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11528778..11548466hg38UCSC Ensembl
chr8:11386287..11405975hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3819689
hg1919689
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1987n209
Supporting Variantsnssv17505571
Samples
Known GenesBLK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847827
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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