A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111918



Internal ID21295184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112918171..112922125hg38UCSC Ensembl
InnerchrX:112161399..112165353hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg383955
hg193955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1271n145
Supporting Variantsnssv14104056, nssv14101783, nssv14101823, nssv14104037, nssv14105029, nssv14105061
Samplessample13, sample369, sample28, sample213, sample187, sample398
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111918
Frequency
Sample Size467
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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