A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578800



Internal ID20951871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49193915..49194193hg38UCSC Ensembl
chr15:49486112..49486390hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238065
Samples
Known GenesGALK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578800
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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