A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101717



Internal ID21281701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5433979..5453731hg38UCSC Ensembl
InnerchrX:5352020..5371772hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3819753
hg1919753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113829
Supporting Variants
Samplessample316
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101717
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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