A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274274



Internal ID20841314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66135753..66136532hg38UCSC Ensembl
chr7:65600740..65601519hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565524
Supporting Variants
Samples
Known GenesCRCP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274274
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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