A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113356



Internal ID21296622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140958061..140994724hg38UCSC Ensembl
InnerchrX:140040226..140076889hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3836664
hg1936664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1283n145
Supporting Variantsnssv14104987, nssv14101820, nssv14104039
Samplessample159, sample13, sample397
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113356
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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