A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566705



Internal ID20939776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80454557..80455431hg38UCSC Ensembl
chr5:79750376..79751250hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268980
Samples
Known GenesZFYVE16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566705
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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