A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250620



Internal ID20817660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64801296..64801444hg38UCSC Ensembl
chr1:65266979..65267127hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538284
Supporting Variants
Samples
Known GenesRAVER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250620
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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