A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253178



Internal ID20820218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77972792..77973038hg38UCSC Ensembl
chr1:78438476..78438722hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550960
Supporting Variants
Samples
Known GenesFUBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253178
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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