A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274640



Internal ID20841680
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 StatusS
Merged Variantsnsv6566345
Supporting Variants
Samples
Known GenesLANCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274640
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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