A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249312



Internal ID20816352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222725024..222725764hg38UCSC Ensembl
chr1:222898366..222899106hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549243
Supporting Variants
Samples
Known GenesBROX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249312
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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