A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117669



Internal ID21300935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:48711167..48715213hg38UCSC Ensembl
InnerchrX:48569558..48573618hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg384047
hg194061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1265n145
Supporting Variantsnssv14101770
Samplessample359
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117669
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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