A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104929



Internal ID21267864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8871614..8889337hg38UCSC Ensembl
InnerchrX:8839655..8857378hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3817724
hg1917724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116269
Supporting Variants
Samplessample118
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104929
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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