A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269434



Internal ID20836474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157801518..157802083hg38UCSC Ensembl
chr5:157228526..157229091hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573463
Supporting Variants
Samples
Known GenesCLINT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269434
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00067


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