A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585529



Internal ID20958600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101770732..101829305hg38UCSC Ensembl
chr15:102310935..102369508hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3858574
hg1958574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238446
Samples
Known GenesOR4F15, OR4F6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585529
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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