A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580324



Internal ID20953395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12331687..12331884hg38UCSC Ensembl
chr18:12331686..12331883hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243431
Samples
Known GenesAFG3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580324
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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