A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250969



Internal ID20818009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42149764..42153647hg38UCSC Ensembl
chr1:42615435..42619318hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg383884
hg193884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542000
Supporting Variants
Samples
Known GenesGUCA2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250969
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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