A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542191



Internal ID20915455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:50522770..50524208hg38UCSC Ensembl
chr2:50749908..50751346hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg381439
hg191439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3863n223
Supporting Variantsnssv18258725
Samples
Known GenesNRXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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