A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876407



Internal ID22651368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101787418..101814246hg38UCSC Ensembl
chr15:102327621..102354449hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3826829
hg1926829
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470704
Samples
Known GenesOR4F6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876407
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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