A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557109



Internal ID20930180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53193121..54035928hg38UCSC Ensembl
chr7:53260814..54103621hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38842808
hg19842808
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274613
Samples
Known GenesFLJ45974
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557109
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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