A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108107



Internal ID22017341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129915281..129915428hg38UCSC Ensembl
chrX:129049257..129049404hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645275
Samples
Known GenesUTP14A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108107
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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