A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226607



Internal ID20793647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15037447..15052905hg38UCSC Ensembl
chr10:15079446..15094904hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3815459
hg1915459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575973
Supporting Variants
Samples
Known GenesOLAH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226607
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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