A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577446



Internal ID20950517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54521354..54521911hg38UCSC Ensembl
chr14:54988072..54988629hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237778
Samples
Known GenesCGRRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577446
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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