A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563120



Internal ID20936191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61840493..62571231hg38UCSC Ensembl
chr4:62706211..63436949hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38730739
hg19730739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265878
Samples
Known GenesLPHN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563120
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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