A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251154



Internal ID20818194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47291125..47291662hg38UCSC Ensembl
chr1:47756797..47757334hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545964
Supporting Variants
Samples
Known GenesSTIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251154
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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