A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv819n223



Internal ID22803787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79533787..80226633hg38UCSC Ensembl
chr10:81293543..81986389hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38692847
hg19692847
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6587639, nsv6595201, nsv6575760, nsv6586915
Samples
Known GenesANXA11, BEND3P3, LINC00857, LOC100288974, LOC642361, MBL1P, NUTM2B, PLAC9, SFTPA1, SFTPA2, SFTPD, TMEM254, TMEM254-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv819n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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