A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278137



Internal ID20845177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48622203..48622785hg38UCSC Ensembl
chr8:49534763..49535345hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572542
Supporting Variants
Samples
Known GenesLOC101929217, LOC101929268
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278137
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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