A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101837



Internal ID21287707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:118224477..118229914hg38UCSC Ensembl
InnerchrX:117358440..117363877hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg385438
hg195438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118012
Supporting Variants
Samplessample405
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101837
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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