A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101723



Internal ID21282092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:49787704..49797683hg38UCSC Ensembl
InnerchrX:49552307..49562286hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg389980
hg199980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113225
Supporting Variants
Samplessample321
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101723
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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