A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566345



Internal ID20939416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55419822..55434020hg38UCSC Ensembl
chr7:55487515..55501713hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3814199
hg1914199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274640
Samples
Known GenesLANCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566345
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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