A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248151



Internal ID20815191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151435996..151437038hg38UCSC Ensembl
chr1:151408472..151409514hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381043
hg191043
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546446
Supporting Variants
Samples
Known GenesPOGZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248151
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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