A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764007



Internal ID20539867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138908023..138908139hg38UCSC Ensembl
chrX:137990185..137990301hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265809
Samples
Known GenesFGF13
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764007
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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