A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645275



Internal ID21837322
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 StatusS
Merged Variantsnsv6108107
Supporting Variants
Samples
Known GenesUTP14A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645275
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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