A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228542



Internal ID20795582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25058223..25058931hg38UCSC Ensembl
chr10:25347152..25347860hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584014
Supporting Variants
Samples
Known GenesENKUR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228542
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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