A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272673



Internal ID20839713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22824577..22825584hg38UCSC Ensembl
chr7:22864196..22865203hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381008
hg191008
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272673
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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