A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591816



Internal ID20964887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64654176..64654850hg38UCSC Ensembl
chr12:65047956..65048630hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1571n223
Supporting Variantsnssv18224167
Samples
Known GenesRASSF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591816
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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