A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583245



Internal ID20956316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33291921..33292691hg38UCSC Ensembl
chr10:33580849..33581619hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38771
hg19771
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231393
Samples
Known GenesNRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583245
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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