A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580376



Internal ID20953447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44410721..44411117hg38UCSC Ensembl
chr15:44702919..44703315hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240234
Samples
Known GenesCASC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580376
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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