A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583708



Internal ID20956779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44544099..44544703hg38UCSC Ensembl
chr15:44836297..44836901hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240255
Samples
Known GenesEIF3J
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583708
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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