A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849383



Internal ID22624318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54022995..54026994hg38UCSC Ensembl
chr8:54935555..54939554hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849383
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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