A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226412



Internal ID20793452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33280916..33281227hg38UCSC Ensembl
chr10:33569844..33570155hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581834
Supporting Variants
Samples
Known GenesNRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226412
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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