A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272666



Internal ID20839706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22481389..22816508hg38UCSC Ensembl
chr7:22521008..22856127hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38335120
hg19335120
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573963
Supporting Variants
Samples
Known GenesIL6, LOC100506178, STEAP1B, TOMM7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272666
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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