A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101709



Internal ID21281391
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 StatusS
Merged Variantsnsv3117190
Supporting Variants
Samplessample310
Known GenesLOC100873065
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101709
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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