A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591339



Internal ID20964410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40912497..41102408hg38UCSC Ensembl
chr15:41204695..41394606hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38189912
hg19189912
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238283
Samples
Known GenesCHAC1, DLL4, INO80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591339
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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