A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268796



Internal ID20478014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154341435..154390706hg38UCSC Ensembl
chrX:153569785..153619048hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3849272
hg1949264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765964
Supporting Variants
Samples
Known GenesEMD, FLNA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268796
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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