A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872786



Internal ID22647727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89477429..89522528hg38UCSC Ensembl
chr15:90020660..90065759hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3845100
hg1945100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474360
Samples
Known GenesLINC00928, RHCG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872786
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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