A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101635



Internal ID21278304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:131165211..131169253hg38UCSC Ensembl
InnerchrX:130299185..130303227hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg384043
hg194043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115537
Supporting Variants
Samplessample267
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101635
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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