A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759341



Internal ID20535201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119647909..119647909hg38UCSC Ensembl
chrX:118781872..118781872hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271664
Samples
Known GenesSEPT6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759341
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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