A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969224



Internal ID22744159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101770737..101829305hg38UCSC Ensembl
chr15:102310940..102369508hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3858569
hg1958569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374379
Samples
Known GenesOR4F15, OR4F6
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969224
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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