A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572212



Internal ID20945283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79316623..79317930hg38UCSC Ensembl
chr5:78612446..78613753hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270294
Samples
Known GenesJMY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572212
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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