A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101663



Internal ID21279431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141441280..141675983hg38UCSC Ensembl
InnerchrX:140529267..140764141hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38234704
hg19234875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111609
Supporting Variants
Samplessample283
Known GenesSPANXA1, SPANXA2, SPANXA2-OT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101663
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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