A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114497



Internal ID21297763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15881987..15910235hg38UCSC Ensembl
InnerchrX:15900110..15928358hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3828249
hg1928249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104963
Samplessample145
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114497
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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