A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768261



Internal ID20544121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129916039..129916197hg38UCSC Ensembl
chrX:129050015..129050173hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283285
Samples
Known GenesUTP14A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768261
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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