A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278149



Internal ID20845189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:49928127..49928270hg38UCSC Ensembl
chr8:50840687..50840830hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574876
Supporting Variants
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278149
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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