A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538290



Internal ID20856974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51796671..51797208hg38UCSC Ensembl
chr1:52262343..52262880hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249672
Samples
Known GenesNRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538290
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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