A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274454



Internal ID20841494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14052897..14065310hg38UCSC Ensembl
chr7:14092522..14104935hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3812414
hg1912414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563766
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274454
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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