A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864485



Internal ID22639420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80877943..80879942hg38UCSC Ensembl
chr9:83492858..83494857hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864485
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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