A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247139



Internal ID20814179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155797856..155798577hg38UCSC Ensembl
chr1:155767647..155768368hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535617
Supporting Variants
Samples
Known GenesGON4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247139
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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