A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591395



Internal ID20964466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52177068..52177470hg38UCSC Ensembl
chr15:52469265..52469667hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240371
Samples
Known GenesGNB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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