A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267614



Internal ID20834654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169129363..169130038hg38UCSC Ensembl
chr5:168556368..168557043hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560280
Supporting Variants
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267614
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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