A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267449



Internal ID20834489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160675362..160679032hg38UCSC Ensembl
chr5:160102369..160106039hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg383671
hg193671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561558
Supporting Variants
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267449
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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