A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv131n223



Internal ID22803099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25283667..25409783hg38UCSC Ensembl
chr1:25610158..25736274hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38126117
hg19126117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6538519, nsv6542632
Samples
Known GenesRHCE, RHD, TMEM50A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv131n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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