A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1265n145



Internal ID22814281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48711167..48715835hg38UCSC Ensembl
chrX:48569558..48574240hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg384669
hg194683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117669, nsv3115430
Samplessample359, sample321
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1265n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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