A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251353



Internal ID20818393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70463958..70464422hg38UCSC Ensembl
chr1:70929641..70930105hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546508
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251353
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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