A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249672



Internal ID20816712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51796671..51797208hg38UCSC Ensembl
chr1:52262343..52262880hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538290
Supporting Variants
Samples
Known GenesNRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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