A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110795



Internal ID21294061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:145834951..145843627hg38UCSC Ensembl
InnerchrX:144916469..144925145hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg388677
hg198677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104989
Samplessample160
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110795
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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