A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274478



Internal ID20841518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140984092..140985621hg38UCSC Ensembl
chr7:140683892..140685421hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381530
hg191530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566792
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274478
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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