A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225613



Internal ID20792653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26903566..27312250hg38UCSC Ensembl
chr10:27192495..27601179hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38408685
hg19408685
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586792
Supporting Variants
Samples
Known GenesACBD5, ANKRD26, LINC00202-1, LRRC37A6P, MASTL, YME1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225613
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.17753


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