A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287660



Internal ID20496878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154347246..154384863hg38UCSC Ensembl
chrX:153575614..153613223hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3837618
hg1937610
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759177
Supporting Variants
Samples
Known GenesEMD, FLNA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287660
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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