A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581450



Internal ID20954521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41214439..41214895hg38UCSC Ensembl
chr15:41506637..41507093hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238311
Samples
Known GenesEXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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