A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117190



Internal ID21300456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:23143824..23161094hg38UCSC Ensembl
InnerchrX:23161941..23179211hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3817271
hg1917271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101709
Samplessample310
Known GenesLOC100873065
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117190
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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