A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251259



Internal ID20818299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67122093..67123199hg38UCSC Ensembl
chr1:67587776..67588882hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381107
hg191107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548301
Supporting Variants
Samples
Known GenesC1orf141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251259
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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