A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114718



Internal ID21297984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32120551..32122368hg38UCSC Ensembl
InnerchrX:32138668..32140485hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg381818
hg191818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101795
Samplessample381
Known GenesDMD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114718
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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