A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856810



Internal ID22631745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122853637..122861736hg38UCSC Ensembl
chr9:125615916..125624015hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg388100
hg198100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511265
Samples
Known GenesRC3H2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856810
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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