A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849522



Internal ID22624457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11646008..11667951hg38UCSC Ensembl
chr8:11503517..11525460hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3821944
hg1921944
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849522
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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