A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250382



Internal ID20817422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231830779..232122782hg38UCSC Ensembl
chr1:231966525..232258528hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38292004
hg19292004
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553486
Supporting Variants
Samples
Known GenesDISC1, TSNAX-DISC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250382
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00019


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