A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv81n199



Internal ID22802967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154335917..154396246hg38UCSC Ensembl
chrX:153564267..153624587hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3860330
hg1960321
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4765964, nsv4764227, nsv4754021
Samples
Known GenesEMD, FLNA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv81n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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