A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845700



Internal ID22620635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7409588..7410907hg38UCSC Ensembl
chr6:7409821..7411140hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg381320
hg191320
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507983
Samples
Known GenesRIOK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845700
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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