A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116269



Internal ID21299535
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 StatusM
Merged Variants
Supporting Variantsnssv14104929
Samplessample118
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116269
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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