A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765964



Internal ID20541824
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 StatusM
Merged Variantsdgv81n199
Supporting Variantsnssv16268796
Samples
Known GenesEMD, FLNA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765964
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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