A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863677



Internal ID22638612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133153929..133158729hg38UCSC Ensembl
chr9:136029316..136034116hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg384801
hg194801
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511644
Samples
Known GenesGBGT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863677
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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