A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541190



Internal ID20914474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113885175..113885756hg38UCSC Ensembl
chr1:114427797..114428378hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249234
Samples
Known GenesAP4B1-AS1, BCL2L15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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