A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116451



Internal ID21299717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140716246..140730776hg38UCSC Ensembl
InnerchrX:139798411..139812941hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3814531
hg1914531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101727
Samplessample321
Known GenesLINC00632
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116451
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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