A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101743



Internal ID21283134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:38937062..39871734hg38UCSC Ensembl
InnerchrX:38796316..39730988hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38934673
hg19934673
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117227
Supporting Variants
Samplessample339
Known GenesLOC286442
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101743
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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