A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250717



Internal ID20817757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235542585..235549050hg38UCSC Ensembl
chr1:235705885..235712350hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg386466
hg196466
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554115
Supporting Variants
Samples
Known GenesGNG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250717
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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