A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104864



Internal ID22014097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:139179053..139194381hg38UCSC Ensembl
chrX:138261215..138276543hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3815329
hg1915329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642266
Samples
Known GenesFGF13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104864
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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