A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646295



Internal ID21838342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45155063..45155197hg38UCSC Ensembl
chrX:45014308..45014442hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112610
Supporting Variants
Samples
Known GenesCXorf36
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646295
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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