A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591363



Internal ID20964434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43091143..43091607hg38UCSC Ensembl
chr15:43383341..43383805hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2508n223
Supporting Variantsnssv18239551
Samples
Known GenesUBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591363
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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